##gff-version 3
##gvf-version 1.07
##file-date 2020-05-22
##genome-build ensembl ASM465v1
##species http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=39946
##feature-ontology http://song.cvs.sourceforge.net/viewvc/song/ontology/so.obo?revision=1.283
##data-source Source=ensembl;version=101;url=http://plants.ensembl.org/Oryza_sativa_Indica_Group
##file-version 101
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##sequence-region AAAA02039986.1 1 5641
##sequence-region AAAA02041781.1 1 4380
##sequence-region CH398810.1 1 9743
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##sequence-region AAAA02035704.1 1 36948
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##sequence-region AAAA02046924.1 1 2584
##sequence-region CH398687.1 1 11178
##sequence-region AAAA02046577.1 1 2666
##sequence-region AAAA02045347.1 1 2977
##sequence-region CH399953.1 1 4111
##sequence-region AAAA02046096.1 1 2788
##sequence-region AAAA02043076.1 1 3722
##sequence-region AAAA02044691.1 1 3152
##sequence-region AAAA02048050.1 1 2357
##sequence-region AAAA02040578.1 1 5142
##sequence-region AAAA02038195.1 1 8398
##sequence-region AAAA02042109.1 1 4185
##sequence-region AAAA02047541.1 1 2446
##sequence-region AAAA02040650.1 1 5101
##sequence-region CH398623.1 1 12101
##sequence-region CH399479.1 1 5446
##sequence-region CH398957.1 1 8278
##sequence-region AAAA02050151.1 1 2011
##sequence-region AAAA02043725.1 1 3461
##sequence-region CH400365.1 1 3167
##sequence-region AAAA02048341.1 1 2302
##sequence-region AAAA02044529.1 1 3201
##sequence-region CH400732.1 1 2560
##sequence-region AAAA02046180.1 1 2767
##sequence-region CH398904.1 1 8684
##sequence-region AAAA02041188.1 1 4732
##sequence-region AAAA02040268.1 1 5376
##sequence-region CH398448.1 1 17730
##sequence-region AAAA02043098.1 1 3715
##sequence-region CH400367.1 1 3166
##sequence-region CH398274.1 1 35921
##sequence-region AAAA02041848.1 1 4339
##sequence-region CH398648.1 1 11780
##sequence-region AAAA02048413.1 1 2287
##sequence-region AAAA02048335.1 1 2302
##sequence-region AAAA02049767.1 1 2070
##sequence-region AAAA02041184.1 1 4734
##sequence-region AAAA02042096.1 1 4188
##sequence-region AAAA02045830.1 1 2846
##sequence-region AAAA02045866.1 1 2835
##sequence-region CH399865.1 1 4286
##sequence-region AAAA02041044.1 1 4817
##sequence-region AAAA02041021.1 1 4845
##sequence-region CH398688.1 1 11177
##sequence-region AAAA02045494.1 1 2931
##sequence-region AAAA02039098.1 1 6829
##sequence-region CH399445.1 1 5563
##sequence-region CH398360.1 1 22107
##sequence-region CH400105.1 1 3709
##sequence-region CH400193.1 1 3518
##sequence-region AAAA02037823.1 1 9524
##sequence-region AAAA02049225.1 1 2159
##sequence-region AAAA02039314.1 1 6467
##sequence-region AAAA02045608.1 1 2902
##sequence-region AAAA02041032.1 1 4829
##sequence-region AAAA02043974.1 1 3384
##sequence-region AAAA02038379.1 1 7973
##sequence-region AAAA02037932.1 1 9128
##sequence-region AAAA02047966.1 1 2369
##sequence-region AAAA02042145.1 1 4163
##sequence-region AAAA02043740.1 1 3452
##sequence-region AAAA02048142.1 1 2339
##sequence-region AAAA02038808.1 1 7212
##sequence-region AAAA02045176.1 1 3027
##sequence-region CH400786.1 1 2455
##sequence-region AAAA02041541.1 1 4517
##sequence-region AAAA02041459.1 1 4575
##sequence-region CH400596.1 1 2783
##sequence-region CH398996.1 1 7911
##sequence-region AAAA02046752.1 1 2624
##sequence-region CH399443.1 1 5569
##sequence-region CH399088.1 1 7347
##sequence-region CH399009.1 1 7842
##sequence-region AAAA02044083.1 1 3344
##sequence-region CH399035.1 1 7676
##sequence-region AAAA02039652.1 1 6017
##sequence-region CH400131.1 1 3656
##sequence-region AAAA02041033.1 1 4828
##sequence-region AAAA02039062.1 1 6873
##sequence-region AAAA02046802.1 1 2614
##sequence-region AAAA02037279.1 1 11506
##sequence-region AAAA02046578.1 1 2666
##sequence-region 7 1 27957088
##sequence-region AAAA02046569.1 1 2669
##sequence-region CH399118.1 1 7193
##sequence-region AAAA02047489.1 1 2455
##sequence-region AAAA02039730.1 1 5929
##sequence-region AAAA02045423.1 1 2953
##sequence-region AAAA02048103.1 1 2346
##sequence-region CH398854.1 1 9173
##sequence-region CH398799.1 1 9843
##sequence-region AAAA02044779.1 1 3126
##sequence-region AAAA02050091.1 1 2020
##sequence-region AAAA02041666.1 1 4443
##sequence-region AAAA02044592.1 1 3183
##sequence-region AAAA02042518.1 1 3995
##sequence-region CH401150.1 1 2011
##sequence-region AAAA02042487.1 1 4010
##sequence-region AAAA02037692.1 1 9955
##sequence-region AAAA02036762.1 1 14978
##sequence-region AAAA02048465.1 1 2279
##sequence-region CH400050.1 1 3829
##sequence-region AAAA02048317.1 1 2305
##sequence-region CH399911.1 1 4167
##sequence-region AAAA02046498.1 1 2686
##sequence-region AAAA02042054.1 1 4214
##sequence-region AAAA02046529.1 1 2678
##sequence-region CH399106.1 1 7251
##sequence-region CH400685.1 1 2639
##sequence-region CH399161.1 1 6988
##sequence-region AAAA02047498.1 1 2454
##sequence-region CH400300.1 1 3310
##sequence-region AAAA02047991.1 1 2364
##sequence-region AAAA02047087.1 1 2545
##sequence-region CH398273.1 1 35942
##sequence-region AAAA02041876.1 1 4318
##sequence-region CH400648.1 1 2704
##sequence-region AAAA02041443.1 1 4593
##sequence-region AAAA02043868.1 1 3410
##sequence-region AAAA02042284.1 1 4118
##sequence-region CH400036.1 1 3851
##sequence-region AAAA02040898.1 1 4920
##sequence-region AAAA02044054.1 1 3351
##sequence-region CH399198.1 1 6821
##sequence-region AAAA02046862.1 1 2599
##sequence-region CH400735.1 1 2556
##sequence-region AAAA02040790.1 1 4992
##sequence-region CH398317.1 1 26473
##sequence-region AAAA02039768.1 1 5885
##sequence-region AAAA02042060.1 1 4212
##sequence-region CH398251.1 1 49974
##sequence-region AAAA02045756.1 1 2863
##sequence-region AAAA02042625.1 1 3938
##sequence-region CH399248.1 1 6575
##sequence-region CH399211.1 1 6760
##sequence-region CH398560.1 1 13849
##sequence-region AAAA02046514.1 1 2681
##sequence-region CH400390.1 1 3119
##sequence-region AAAA02047522.1 1 2450
##sequence-region AAAA02045323.1 1 2984
##sequence-region AAAA02044540.1 1 3197
##sequence-region AAAA02038243.1 1 8303
##sequence-region CH399041.1 1 7629
##sequence-region CH398771.1 1 10187
##sequence-region AAAA02036494.1 1 17388
##sequence-region CH398246.1 1 53556
##sequence-region AAAA02040684.1 1 5069
##sequence-region AAAA02040789.1 1 4992
##sequence-region AAAA02047265.1 1 2506
##sequence-region AAAA02042205.1 1 4142
##sequence-region CH398888.1 1 8804
##sequence-region AAAA02039649.1 1 6023
##sequence-region AAAA02042948.1 1 3779
##sequence-region AAAA02040871.1 1 4938
##sequence-region CH398346.1 1 23602
##sequence-region AAAA02044558.1 1 3192
##sequence-region AAAA02047930.1 1 2376
##sequence-region CH399252.1 1 6534
##sequence-region AAAA02039444.1 1 6283
##sequence-region CH399209.1 1 6769
##sequence-region CH398663.1 1 11533
##sequence-region AAAA02042496.1 1 4005
##sequence-region AAAA02049809.1 1 2063
##sequence-region CH400161.1 1 3584
##sequence-region AAAA02048430.1 1 2284
##sequence-region AAAA02037268.1 1 11524
##sequence-region AAAA02042584.1 1 3963
##sequence-region AAAA02043695.1 1 3478
##sequence-region AAAA02050033.1 1 2028
##sequence-region CH400221.1 1 3449
##sequence-region CH398924.1 1 8518
##sequence-region AAAA02040591.1 1 5133
##sequence-region AAAA02043398.1 1 3592
##sequence-region CH398800.1 1 9806
##sequence-region AAAA02043984.1 1 3378
##sequence-region AAAA02040503.1 1 5200
##sequence-region AAAA02044857.1 1 3106
##sequence-region AAAA02046229.1 1 2756
##sequence-region CH399356.1 1 5949
##sequence-region AAAA02039351.1 1 6403
##sequence-region AAAA02040434.1 1 5253
##sequence-region AAAA02039701.1 1 5957
##sequence-region AAAA02044242.1 1 3295
##sequence-region AAAA02036585.1 1 16710
##sequence-region AAAA02039964.1 1 5664
##sequence-region AAAA02035612.1 1 43555
##sequence-region AAAA02049249.1 1 2155
##sequence-region AAAA02044523.1 1 3202
##sequence-region CH399139.1 1 7110
##sequence-region CH399083.1 1 7388
##sequence-region AAAA02037683.1 1 10013
##sequence-region AAAA02036599.1 1 16549
##sequence-region AAAA02036020.1 1 23662
##sequence-region CH399260.1 1 6430
##sequence-region 2 1 38103930
AAAA02039588.1	dbSNP	SNV	5458	5458	.	+	.	ID=1;Variant_seq=A;Dbxref=dbSNP_129:rs19401727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041446.1	dbSNP	SNV	1995	1995	.	+	.	ID=2;Variant_seq=G;Dbxref=dbSNP_129:rs19876550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041446.1	dbSNP	SNV	4166	4166	.	+	.	ID=3;Variant_seq=A;Dbxref=dbSNP_129:rs54395375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046137.1	dbSNP	SNV	367	367	.	+	.	ID=4;Variant_seq=A;Dbxref=dbSNP_129:rs53026346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041318.1	dbSNP	SNV	3158	3158	.	+	.	ID=5;Variant_seq=T;Dbxref=dbSNP_129:rs18419228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400583.1	dbSNP	SNV	214	214	.	+	.	ID=6;Variant_seq=A;Dbxref=dbSNP_129:rs53826975;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400583.1	dbSNP	SNV	218	218	.	+	.	ID=7;Variant_seq=T;Dbxref=dbSNP_129:rs53240659;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400583.1	dbSNP	SNV	230	230	.	+	.	ID=8;Variant_seq=G;Dbxref=dbSNP_129:rs53206816;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400583.1	dbSNP	SNV	238	238	.	+	.	ID=9;Variant_seq=T;Dbxref=dbSNP_129:rs52975620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400583.1	dbSNP	SNV	245	245	.	+	.	ID=10;Variant_seq=A;Dbxref=dbSNP_129:rs53876231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400583.1	dbSNP	SNV	254	254	.	+	.	ID=11;Variant_seq=C;Dbxref=dbSNP_129:rs53730242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400583.1	dbSNP	SNV	261	261	.	+	.	ID=12;Variant_seq=T;Dbxref=dbSNP_129:rs52848055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047275.1	dbSNP	SNV	806	806	.	+	.	ID=13;Variant_seq=A;Dbxref=dbSNP_129:rs54166347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047275.1	dbSNP	SNV	808	808	.	+	.	ID=14;Variant_seq=C;Dbxref=dbSNP_129:rs53219239;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047275.1	dbSNP	SNV	809	809	.	+	.	ID=15;Variant_seq=G;Dbxref=dbSNP_129:rs54303761;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047275.1	dbSNP	SNV	847	847	.	+	.	ID=16;Variant_seq=A;Dbxref=dbSNP_129:rs53885081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041570.1	dbSNP	SNV	405	405	.	+	.	ID=17;Variant_seq=A;Dbxref=dbSNP_129:rs19516650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041570.1	dbSNP	SNV	681	681	.	+	.	ID=18;Variant_seq=G;Dbxref=dbSNP_129:rs52895744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041570.1	dbSNP	SNV	2270	2270	.	+	.	ID=19;Variant_seq=A;Dbxref=dbSNP_129:rs53911551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041570.1	dbSNP	SNV	2277	2277	.	+	.	ID=20;Variant_seq=C;Dbxref=dbSNP_129:rs53272068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041570.1	dbSNP	SNV	2308	2308	.	+	.	ID=21;Variant_seq=T;Dbxref=dbSNP_129:rs53136123;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041570.1	dbSNP	SNV	2314	2314	.	+	.	ID=22;Variant_seq=A;Dbxref=dbSNP_129:rs54360439;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037229.1	dbSNP	SNV	792	792	.	+	.	ID=23;Variant_seq=T;Dbxref=dbSNP_129:rs19386945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037229.1	dbSNP	SNV	9074	9074	.	+	.	ID=24;Variant_seq=C;Dbxref=dbSNP_129:rs53305133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037229.1	dbSNP	SNV	9526	9526	.	+	.	ID=25;Variant_seq=A;Dbxref=dbSNP_129:rs20967794;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044476.1	dbSNP	SNV	869	869	.	+	.	ID=26;Variant_seq=A;Dbxref=dbSNP_129:rs20308385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044476.1	dbSNP	SNV	926	926	.	+	.	ID=27;Variant_seq=A;Dbxref=dbSNP_129:rs20308395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044476.1	dbSNP	SNV	936	936	.	+	.	ID=28;Variant_seq=G;Dbxref=dbSNP_129:rs20308405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044476.1	dbSNP	SNV	1044	1044	.	+	.	ID=29;Variant_seq=T;Dbxref=dbSNP_129:rs20308415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044476.1	dbSNP	SNV	1105	1105	.	+	.	ID=30;Variant_seq=A;Dbxref=dbSNP_129:rs20308425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044476.1	dbSNP	SNV	1333	1333	.	+	.	ID=31;Variant_seq=A;Dbxref=dbSNP_129:rs20308455;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044476.1	dbSNP	SNV	1442	1442	.	+	.	ID=32;Variant_seq=A;Dbxref=dbSNP_129:rs53543083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044476.1	dbSNP	SNV	1664	1664	.	+	.	ID=33;Variant_seq=T;Dbxref=dbSNP_129:rs20308495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044476.1	dbSNP	SNV	1840	1840	.	+	.	ID=34;Variant_seq=G;Dbxref=dbSNP_129:rs20308535;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044476.1	dbSNP	SNV	1919	1919	.	+	.	ID=35;Variant_seq=G;Dbxref=dbSNP_129:rs20308545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044476.1	dbSNP	SNV	1929	1929	.	+	.	ID=36;Variant_seq=A;Dbxref=dbSNP_129:rs20308555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044476.1	dbSNP	SNV	2019	2019	.	+	.	ID=37;Variant_seq=T;Dbxref=dbSNP_129:rs20308565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044476.1	dbSNP	SNV	2945	2945	.	+	.	ID=38;Variant_seq=T;Dbxref=dbSNP_129:rs20308635;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398742.1	dbSNP	SNV	366	366	.	+	.	ID=39;Variant_seq=T;Dbxref=dbSNP_129:rs21241645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398742.1	dbSNP	SNV	3514	3514	.	+	.	ID=40;Variant_seq=A;Dbxref=dbSNP_129:rs20753980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398742.1	dbSNP	SNV	6153	6153	.	+	.	ID=41;Variant_seq=T;Dbxref=dbSNP_129:rs21507794;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398742.1	dbSNP	SNV	6719	6719	.	+	.	ID=42;Variant_seq=T;Dbxref=dbSNP_129:rs21150765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398742.1	dbSNP	SNV	6720	6720	.	+	.	ID=43;Variant_seq=A;Dbxref=dbSNP_129:rs21150775;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398742.1	dbSNP	SNV	6721	6721	.	+	.	ID=44;Variant_seq=C;Dbxref=dbSNP_129:rs21150785;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398742.1	dbSNP	SNV	6864	6864	.	+	.	ID=45;Variant_seq=T;Dbxref=dbSNP_129:rs20354938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398742.1	dbSNP	SNV	8471	8471	.	+	.	ID=46;Variant_seq=T;Dbxref=dbSNP_129:rs20755320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398742.1	dbSNP	SNV	9041	9041	.	+	.	ID=47;Variant_seq=A;Dbxref=dbSNP_129:rs21251347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398742.1	dbSNP	SNV	9051	9051	.	+	.	ID=48;Variant_seq=T;Dbxref=dbSNP_129:rs21251357;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398742.1	dbSNP	SNV	9173	9173	.	+	.	ID=49;Variant_seq=G;Dbxref=dbSNP_129:rs21251397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039309.1	dbSNP	SNV	5609	5609	.	+	.	ID=50;Variant_seq=T;Dbxref=dbSNP_129:rs19381689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039309.1	dbSNP	SNV	5617	5617	.	+	.	ID=51;Variant_seq=G;Dbxref=dbSNP_129:rs19381679;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039309.1	dbSNP	SNV	5649	5649	.	+	.	ID=52;Variant_seq=T;Dbxref=dbSNP_129:rs19381659;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399109.1	dbSNP	SNV	2020	2020	.	+	.	ID=53;Variant_seq=A;Dbxref=dbSNP_129:rs20807564;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399109.1	dbSNP	SNV	5139	5139	.	+	.	ID=54;Variant_seq=T;Dbxref=dbSNP_129:rs20807484;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399109.1	dbSNP	SNV	6349	6349	.	+	.	ID=55;Variant_seq=T;Dbxref=dbSNP_129:rs20807464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038349.1	dbSNP	SNV	327	327	.	+	.	ID=56;Variant_seq=G;Dbxref=dbSNP_129:rs19410077;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038349.1	dbSNP	SNV	339	339	.	+	.	ID=57;Variant_seq=A;Dbxref=dbSNP_129:rs19410057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047147.1	dbSNP	SNV	1100	1100	.	+	.	ID=58;Variant_seq=A;Dbxref=dbSNP_129:rs53425548;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047147.1	dbSNP	SNV	1108	1108	.	+	.	ID=59;Variant_seq=G;Dbxref=dbSNP_129:rs53849415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047147.1	dbSNP	SNV	1112	1112	.	+	.	ID=60;Variant_seq=C;Dbxref=dbSNP_129:rs53048922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047147.1	dbSNP	SNV	1592	1592	.	+	.	ID=61;Variant_seq=T;Dbxref=dbSNP_129:rs53560162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047147.1	dbSNP	SNV	1614	1614	.	+	.	ID=62;Variant_seq=C;Dbxref=dbSNP_129:rs54012469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047147.1	dbSNP	SNV	1617	1617	.	+	.	ID=63;Variant_seq=T;Dbxref=dbSNP_129:rs53804079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047147.1	dbSNP	SNV	1618	1618	.	+	.	ID=64;Variant_seq=T;Dbxref=dbSNP_129:rs53610667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047147.1	dbSNP	SNV	2207	2207	.	+	.	ID=65;Variant_seq=G;Dbxref=dbSNP_129:rs53964955;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047147.1	dbSNP	SNV	2271	2271	.	+	.	ID=66;Variant_seq=A;Dbxref=dbSNP_129:rs53000981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040728.1	dbSNP	SNV	1064	1064	.	+	.	ID=67;Variant_seq=T;Dbxref=dbSNP_129:rs20774348;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040728.1	dbSNP	SNV	1505	1505	.	+	.	ID=68;Variant_seq=A;Dbxref=dbSNP_129:rs19703797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040728.1	dbSNP	SNV	4045	4045	.	+	.	ID=69;Variant_seq=T;Dbxref=dbSNP_129:rs19573978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049305.1	dbSNP	SNV	842	842	.	+	.	ID=70;Variant_seq=A;Dbxref=dbSNP_129:rs53214531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	846	846	.	+	.	ID=71;Variant_seq=T;Dbxref=dbSNP_129:rs53071948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	925	925	.	+	.	ID=72;Variant_seq=T;Dbxref=dbSNP_129:rs21727769;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1748	1748	.	+	.	ID=73;Variant_seq=A;Dbxref=dbSNP_129:rs53605232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049305.1	dbSNP	SNV	1762	1762	.	+	.	ID=74;Variant_seq=T;Dbxref=dbSNP_129:rs53787394;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1762	1762	.	+	.	ID=75;Variant_seq=A;Dbxref=dbSNP_129:rs53831533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1769	1769	.	+	.	ID=76;Variant_seq=G;Dbxref=dbSNP_129:rs53408258;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049305.1	dbSNP	SNV	1777	1777	.	+	.	ID=77;Variant_seq=C;Dbxref=dbSNP_129:rs53087263;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049305.1	dbSNP	SNV	1780	1780	.	+	.	ID=78;Variant_seq=A;Dbxref=dbSNP_129:rs53760283;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	1787	1787	.	+	.	ID=79;Variant_seq=G;Dbxref=dbSNP_129:rs52841642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049305.1	dbSNP	insertion	1824	1824	.	+	.	ID=80;Variant_seq=C;Dbxref=dbSNP_129:rs53128293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02049305.1	dbSNP	SNV	1828	1828	.	+	.	ID=81;Variant_seq=C;Dbxref=dbSNP_129:rs53545746;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049305.1	dbSNP	SNV	1830	1830	.	+	.	ID=82;Variant_seq=A;Dbxref=dbSNP_129:rs53669388;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	1840	1840	.	+	.	ID=83;Variant_seq=A;Dbxref=dbSNP_129:rs52951408;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	1848	1848	.	+	.	ID=84;Variant_seq=T;Dbxref=dbSNP_129:rs52926587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1856	1856	.	+	.	ID=85;Variant_seq=A;Dbxref=dbSNP_129:rs52907333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	1863	1863	.	+	.	ID=86;Variant_seq=T;Dbxref=dbSNP_129:rs53752211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1868	1868	.	+	.	ID=87;Variant_seq=T;Dbxref=dbSNP_129:rs53739440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049305.1	dbSNP	SNV	1980	1980	.	+	.	ID=88;Variant_seq=A;Dbxref=dbSNP_129:rs53017309;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049305.1	dbSNP	SNV	1983	1983	.	+	.	ID=89;Variant_seq=C;Dbxref=dbSNP_129:rs54360631;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049305.1	dbSNP	SNV	1984	1984	.	+	.	ID=90;Variant_seq=G;Dbxref=dbSNP_129:rs53178163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400590.1	dbSNP	SNV	92	92	.	+	.	ID=91;Variant_seq=G;Dbxref=dbSNP_129:rs19471863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400590.1	dbSNP	SNV	314	314	.	+	.	ID=92;Variant_seq=G;Dbxref=dbSNP_129:rs18864514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400590.1	dbSNP	SNV	397	397	.	+	.	ID=93;Variant_seq=G;Dbxref=dbSNP_129:rs18864504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400590.1	dbSNP	SNV	1105	1105	.	+	.	ID=94;Variant_seq=C;Dbxref=dbSNP_129:rs18864434;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049452.1	dbSNP	SNV	204	204	.	+	.	ID=95;Variant_seq=G;Dbxref=dbSNP_129:rs20368826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036229.1	dbSNP	SNV	4547	4547	.	+	.	ID=96;Variant_seq=T;Dbxref=dbSNP_129:rs53355481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036229.1	dbSNP	deletion	7158	7158	.	+	.	ID=97;Variant_seq=-;Dbxref=dbSNP_129:rs53588728;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036229.1	dbSNP	SNV	10562	10562	.	+	.	ID=98;Variant_seq=A;Dbxref=dbSNP_129:rs19018323;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036229.1	dbSNP	SNV	13469	13469	.	+	.	ID=99;Variant_seq=A;Dbxref=dbSNP_129:rs18424415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036229.1	dbSNP	SNV	13488	13488	.	+	.	ID=100;Variant_seq=A;Dbxref=dbSNP_129:rs53529759;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036229.1	dbSNP	SNV	14378	14378	.	+	.	ID=101;Variant_seq=A;Dbxref=dbSNP_129:rs18478943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036229.1	dbSNP	SNV	14437	14437	.	+	.	ID=102;Variant_seq=A;Dbxref=dbSNP_129:rs18478925;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050129.1	dbSNP	SNV	1061	1061	.	+	.	ID=103;Variant_seq=G;Dbxref=dbSNP_129:rs53504203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050129.1	dbSNP	SNV	1073	1073	.	+	.	ID=104;Variant_seq=C;Dbxref=dbSNP_129:rs54397761;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02050129.1	dbSNP	SNV	1091	1091	.	+	.	ID=105;Variant_seq=A;Dbxref=dbSNP_129:rs53292452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050129.1	dbSNP	SNV	1097	1097	.	+	.	ID=106;Variant_seq=C;Dbxref=dbSNP_129:rs52928153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02050129.1	dbSNP	SNV	1118	1118	.	+	.	ID=107;Variant_seq=C;Dbxref=dbSNP_129:rs53119284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	202	202	.	+	.	ID=108;Variant_seq=T;Dbxref=dbSNP_129:rs21626273;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	215	215	.	+	.	ID=109;Variant_seq=A;Dbxref=dbSNP_129:rs21626309;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	216	216	.	+	.	ID=110;Variant_seq=T;Dbxref=dbSNP_129:rs21626318;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	225	225	.	+	.	ID=111;Variant_seq=T;Dbxref=dbSNP_129:rs19732520;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	244	244	.	+	.	ID=112;Variant_seq=A;Dbxref=dbSNP_129:rs21626336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	438	438	.	+	.	ID=113;Variant_seq=T;Dbxref=dbSNP_129:rs21626408;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	456	456	.	+	.	ID=114;Variant_seq=T;Dbxref=dbSNP_129:rs21626417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	501	501	.	+	.	ID=115;Variant_seq=C;Dbxref=dbSNP_129:rs21626435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	937	937	.	+	.	ID=116;Variant_seq=T;Dbxref=dbSNP_129:rs21626741;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	948	948	.	+	.	ID=117;Variant_seq=G;Dbxref=dbSNP_129:rs21626750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	963	963	.	+	.	ID=118;Variant_seq=T;Dbxref=dbSNP_129:rs21626777;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	965	965	.	+	.	ID=119;Variant_seq=A;Dbxref=dbSNP_129:rs21626786;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1042	1042	.	+	.	ID=120;Variant_seq=T;Dbxref=dbSNP_129:rs21626894;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1043	1043	.	+	.	ID=121;Variant_seq=T;Dbxref=dbSNP_129:rs21626903;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1054	1054	.	+	.	ID=122;Variant_seq=A;Dbxref=dbSNP_129:rs21626921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1057	1057	.	+	.	ID=123;Variant_seq=C;Dbxref=dbSNP_129:rs21626930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1067	1067	.	+	.	ID=124;Variant_seq=T;Dbxref=dbSNP_129:rs21626939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1175	1175	.	+	.	ID=125;Variant_seq=G;Dbxref=dbSNP_129:rs21627010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1189	1189	.	+	.	ID=126;Variant_seq=T;Dbxref=dbSNP_129:rs21627019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	1307	1307	.	+	.	ID=127;Variant_seq=G;Dbxref=dbSNP_129:rs21627127;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	1310	1310	.	+	.	ID=128;Variant_seq=T;Dbxref=dbSNP_129:rs21627136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1324	1324	.	+	.	ID=129;Variant_seq=C;Dbxref=dbSNP_129:rs21627163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	1335	1335	.	+	.	ID=130;Variant_seq=T;Dbxref=dbSNP_129:rs21627181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	1346	1346	.	+	.	ID=131;Variant_seq=T;Dbxref=dbSNP_129:rs21627190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1426	1426	.	+	.	ID=132;Variant_seq=A;Dbxref=dbSNP_129:rs21627217;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1455	1455	.	+	.	ID=133;Variant_seq=A;Dbxref=dbSNP_129:rs21627226;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1565	1565	.	+	.	ID=134;Variant_seq=C;Dbxref=dbSNP_129:rs21627307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	1575	1575	.	+	.	ID=135;Variant_seq=A;Dbxref=dbSNP_129:rs21627325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1578	1578	.	+	.	ID=136;Variant_seq=T;Dbxref=dbSNP_129:rs21627334;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	1579	1579	.	+	.	ID=137;Variant_seq=T;Dbxref=dbSNP_129:rs21627343;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1583	1583	.	+	.	ID=138;Variant_seq=A;Dbxref=dbSNP_129:rs21627352;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	1586	1586	.	+	.	ID=139;Variant_seq=A;Dbxref=dbSNP_129:rs21627370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	2047	2047	.	+	.	ID=140;Variant_seq=A;Dbxref=dbSNP_129:rs53593476;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	2048	2048	.	+	.	ID=141;Variant_seq=A;Dbxref=dbSNP_129:rs52872802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	2056	2056	.	+	.	ID=142;Variant_seq=A;Dbxref=dbSNP_129:rs53821851;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	2057	2057	.	+	.	ID=143;Variant_seq=G;Dbxref=dbSNP_129:rs54199747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	insertion	2711	2711	.	+	.	ID=144;Variant_seq=A;Dbxref=dbSNP_129:rs53329079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02044038.1	dbSNP	SNV	2715	2715	.	+	.	ID=145;Variant_seq=A;Dbxref=dbSNP_129:rs53713520;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	2721	2721	.	+	.	ID=146;Variant_seq=T;Dbxref=dbSNP_129:rs21629551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	2722	2722	.	+	.	ID=147;Variant_seq=T;Dbxref=dbSNP_129:rs21629560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	2739	2739	.	+	.	ID=148;Variant_seq=T;Dbxref=dbSNP_129:rs21629578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044038.1	dbSNP	SNV	2746	2746	.	+	.	ID=149;Variant_seq=A;Dbxref=dbSNP_129:rs54319866;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	2753	2753	.	+	.	ID=150;Variant_seq=G;Dbxref=dbSNP_129:rs21629587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	2753	2753	.	+	.	ID=151;Variant_seq=A;Dbxref=dbSNP_129:rs53157443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044038.1	dbSNP	SNV	2754	2754	.	+	.	ID=152;Variant_seq=A;Dbxref=dbSNP_129:rs53576458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044038.1	dbSNP	SNV	2755	2755	.	+	.	ID=153;Variant_seq=G;Dbxref=dbSNP_129:rs53060165;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044038.1	dbSNP	SNV	2761	2761	.	+	.	ID=154;Variant_seq=T;Dbxref=dbSNP_129:rs53623483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	231	231	.	+	.	ID=155;Variant_seq=T;Dbxref=dbSNP_129:rs53581827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	271	271	.	+	.	ID=156;Variant_seq=T;Dbxref=dbSNP_129:rs53759918;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	392	392	.	+	.	ID=157;Variant_seq=A;Dbxref=dbSNP_129:rs54296836;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043714.1	dbSNP	SNV	401	401	.	+	.	ID=158;Variant_seq=T;Dbxref=dbSNP_129:rs54379644;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	473	473	.	+	.	ID=159;Variant_seq=T;Dbxref=dbSNP_129:rs53149627;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	486	486	.	+	.	ID=160;Variant_seq=G;Dbxref=dbSNP_129:rs53595048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043714.1	dbSNP	SNV	489	489	.	+	.	ID=161;Variant_seq=A;Dbxref=dbSNP_129:rs54137861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043714.1	dbSNP	SNV	502	502	.	+	.	ID=162;Variant_seq=C;Dbxref=dbSNP_129:rs54378272;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043714.1	dbSNP	SNV	2685	2685	.	+	.	ID=163;Variant_seq=T;Dbxref=dbSNP_129:rs20980542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	2689	2689	.	+	.	ID=164;Variant_seq=T;Dbxref=dbSNP_129:rs20980552;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043714.1	dbSNP	SNV	2783	2783	.	+	.	ID=165;Variant_seq=G;Dbxref=dbSNP_129:rs19512195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399025.1	dbSNP	SNV	4543	4543	.	+	.	ID=166;Variant_seq=C;Dbxref=dbSNP_129:rs54299814;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	425	425	.	+	.	ID=167;Variant_seq=T;Dbxref=dbSNP_129:rs21090135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	467	467	.	+	.	ID=168;Variant_seq=G;Dbxref=dbSNP_129:rs21090255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	468	468	.	+	.	ID=169;Variant_seq=A;Dbxref=dbSNP_129:rs21090265;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	479	479	.	+	.	ID=170;Variant_seq=T;Dbxref=dbSNP_129:rs21090275;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	484	484	.	+	.	ID=171;Variant_seq=C;Dbxref=dbSNP_129:rs21090285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	490	490	.	+	.	ID=172;Variant_seq=T;Dbxref=dbSNP_129:rs21090305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	495	495	.	+	.	ID=173;Variant_seq=G;Dbxref=dbSNP_129:rs21090325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	497	497	.	+	.	ID=174;Variant_seq=T;Dbxref=dbSNP_129:rs21090335;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	521	521	.	+	.	ID=175;Variant_seq=G;Dbxref=dbSNP_129:rs21090345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	529	529	.	+	.	ID=176;Variant_seq=G;Dbxref=dbSNP_129:rs21090375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	530	530	.	+	.	ID=177;Variant_seq=A;Dbxref=dbSNP_129:rs21090385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	532	532	.	+	.	ID=178;Variant_seq=A;Dbxref=dbSNP_129:rs21090395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	573	573	.	+	.	ID=179;Variant_seq=T;Dbxref=dbSNP_129:rs21090445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	597	597	.	+	.	ID=180;Variant_seq=C;Dbxref=dbSNP_129:rs21090505;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	620	620	.	+	.	ID=181;Variant_seq=C;Dbxref=dbSNP_129:rs21090525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	656	656	.	+	.	ID=182;Variant_seq=G;Dbxref=dbSNP_129:rs21090585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	840	840	.	+	.	ID=183;Variant_seq=C;Dbxref=dbSNP_129:rs21090695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	841	841	.	+	.	ID=184;Variant_seq=T;Dbxref=dbSNP_129:rs21090705;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	867	867	.	+	.	ID=185;Variant_seq=C;Dbxref=dbSNP_129:rs21090715;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	878	878	.	+	.	ID=186;Variant_seq=A;Dbxref=dbSNP_129:rs21090735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	889	889	.	+	.	ID=187;Variant_seq=A;Dbxref=dbSNP_129:rs21090745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	898	898	.	+	.	ID=188;Variant_seq=A;Dbxref=dbSNP_129:rs21090755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	899	899	.	+	.	ID=189;Variant_seq=T;Dbxref=dbSNP_129:rs21090765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	971	971	.	+	.	ID=190;Variant_seq=T;Dbxref=dbSNP_129:rs21090825;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	985	985	.	+	.	ID=191;Variant_seq=T;Dbxref=dbSNP_129:rs21090845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044272.1	dbSNP	SNV	988	988	.	+	.	ID=192;Variant_seq=A;Dbxref=dbSNP_129:rs21090855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	989	989	.	+	.	ID=193;Variant_seq=T;Dbxref=dbSNP_129:rs21090865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	996	996	.	+	.	ID=194;Variant_seq=C;Dbxref=dbSNP_129:rs21090895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044272.1	dbSNP	SNV	997	997	.	+	.	ID=195;Variant_seq=G;Dbxref=dbSNP_129:rs21090905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	998	998	.	+	.	ID=196;Variant_seq=C;Dbxref=dbSNP_129:rs21090915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	1000	1000	.	+	.	ID=197;Variant_seq=A;Dbxref=dbSNP_129:rs21090925;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	1009	1009	.	+	.	ID=198;Variant_seq=T;Dbxref=dbSNP_129:rs21090945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044272.1	dbSNP	SNV	1019	1019	.	+	.	ID=199;Variant_seq=T;Dbxref=dbSNP_129:rs21090955;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044272.1	dbSNP	SNV	2507	2507	.	+	.	ID=200;Variant_seq=G;Dbxref=dbSNP_129:rs54312745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	465	465	.	+	.	ID=201;Variant_seq=A;Dbxref=dbSNP_129:rs20292106;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	471	471	.	+	.	ID=202;Variant_seq=T;Dbxref=dbSNP_129:rs20292076;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	478	478	.	+	.	ID=203;Variant_seq=A;Dbxref=dbSNP_129:rs20292056;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	483	483	.	+	.	ID=204;Variant_seq=T;Dbxref=dbSNP_129:rs20292036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	484	484	.	+	.	ID=205;Variant_seq=T;Dbxref=dbSNP_129:rs20292026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	489	489	.	+	.	ID=206;Variant_seq=T;Dbxref=dbSNP_129:rs20291996;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	490	490	.	+	.	ID=207;Variant_seq=A;Dbxref=dbSNP_129:rs20291986;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	502	502	.	+	.	ID=208;Variant_seq=A;Dbxref=dbSNP_129:rs20291906;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	508	508	.	+	.	ID=209;Variant_seq=G;Dbxref=dbSNP_129:rs20291896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	513	513	.	+	.	ID=210;Variant_seq=C;Dbxref=dbSNP_129:rs20291876;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	519	519	.	+	.	ID=211;Variant_seq=C;Dbxref=dbSNP_129:rs20291846;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	525	525	.	+	.	ID=212;Variant_seq=T;Dbxref=dbSNP_129:rs20291826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	531	531	.	+	.	ID=213;Variant_seq=T;Dbxref=dbSNP_129:rs20291796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	544	544	.	+	.	ID=214;Variant_seq=A;Dbxref=dbSNP_129:rs20291726;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	549	549	.	+	.	ID=215;Variant_seq=T;Dbxref=dbSNP_129:rs20291696;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	555	555	.	+	.	ID=216;Variant_seq=T;Dbxref=dbSNP_129:rs20291656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	562	562	.	+	.	ID=217;Variant_seq=T;Dbxref=dbSNP_129:rs20291626;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	585	585	.	+	.	ID=218;Variant_seq=A;Dbxref=dbSNP_129:rs20291526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	591	591	.	+	.	ID=219;Variant_seq=T;Dbxref=dbSNP_129:rs20291486;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	712	712	.	+	.	ID=220;Variant_seq=T;Dbxref=dbSNP_129:rs20291047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	742	742	.	+	.	ID=221;Variant_seq=C;Dbxref=dbSNP_129:rs20290927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	760	760	.	+	.	ID=222;Variant_seq=T;Dbxref=dbSNP_129:rs20290837;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	861	861	.	+	.	ID=223;Variant_seq=C;Dbxref=dbSNP_129:rs20290207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	862	862	.	+	.	ID=224;Variant_seq=T;Dbxref=dbSNP_129:rs20290197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	868	868	.	+	.	ID=225;Variant_seq=C;Dbxref=dbSNP_129:rs20290157;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	873	873	.	+	.	ID=226;Variant_seq=C;Dbxref=dbSNP_129:rs20290127;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	886	886	.	+	.	ID=227;Variant_seq=C;Dbxref=dbSNP_129:rs20290047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	903	903	.	+	.	ID=228;Variant_seq=T;Dbxref=dbSNP_129:rs20289957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	915	915	.	+	.	ID=229;Variant_seq=T;Dbxref=dbSNP_129:rs20289897;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	921	921	.	+	.	ID=230;Variant_seq=T;Dbxref=dbSNP_129:rs20289848;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	934	934	.	+	.	ID=231;Variant_seq=C;Dbxref=dbSNP_129:rs20289798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	945	945	.	+	.	ID=232;Variant_seq=T;Dbxref=dbSNP_129:rs20289738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047863.1	dbSNP	SNV	952	952	.	+	.	ID=233;Variant_seq=T;Dbxref=dbSNP_129:rs20289698;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	994	994	.	+	.	ID=234;Variant_seq=A;Dbxref=dbSNP_129:rs20289508;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	1059	1059	.	+	.	ID=235;Variant_seq=C;Dbxref=dbSNP_129:rs20289228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047863.1	dbSNP	SNV	1065	1065	.	+	.	ID=236;Variant_seq=A;Dbxref=dbSNP_129:rs20289188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047863.1	dbSNP	SNV	1071	1071	.	+	.	ID=237;Variant_seq=A;Dbxref=dbSNP_129:rs20289168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045339.1	dbSNP	SNV	2085	2085	.	+	.	ID=238;Variant_seq=A;Dbxref=dbSNP_129:rs18090965;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046722.1	dbSNP	SNV	300	300	.	+	.	ID=239;Variant_seq=C;Dbxref=dbSNP_129:rs20076189;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399350.1	dbSNP	SNV	4034	4034	.	+	.	ID=240;Variant_seq=T;Dbxref=dbSNP_129:rs19474896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400690.1	dbSNP	SNV	190	190	.	+	.	ID=241;Variant_seq=G;Dbxref=dbSNP_129:rs19936378;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400690.1	dbSNP	SNV	201	201	.	+	.	ID=242;Variant_seq=C;Dbxref=dbSNP_129:rs19936398;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400690.1	dbSNP	SNV	207	207	.	+	.	ID=243;Variant_seq=C;Dbxref=dbSNP_129:rs19936418;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400690.1	dbSNP	SNV	208	208	.	+	.	ID=244;Variant_seq=T;Dbxref=dbSNP_129:rs19936428;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400690.1	dbSNP	SNV	210	210	.	+	.	ID=245;Variant_seq=G;Dbxref=dbSNP_129:rs19936438;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400690.1	dbSNP	SNV	213	213	.	+	.	ID=246;Variant_seq=G;Dbxref=dbSNP_129:rs19936448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400690.1	dbSNP	SNV	2356	2356	.	+	.	ID=247;Variant_seq=A;Dbxref=dbSNP_129:rs54391335;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400477.1	dbSNP	SNV	989	989	.	+	.	ID=248;Variant_seq=A;Dbxref=dbSNP_129:rs53834664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036929.1	dbSNP	SNV	5493	5493	.	+	.	ID=249;Variant_seq=T;Dbxref=dbSNP_129:rs18169646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036929.1	dbSNP	SNV	7248	7248	.	+	.	ID=250;Variant_seq=T;Dbxref=dbSNP_129:rs21359306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036929.1	dbSNP	SNV	7990	7990	.	+	.	ID=251;Variant_seq=A;Dbxref=dbSNP_129:rs21361238;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	192	192	.	+	.	ID=252;Variant_seq=A;Dbxref=dbSNP_129:rs53729149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	274	274	.	+	.	ID=253;Variant_seq=G;Dbxref=dbSNP_129:rs54211767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399471.1	dbSNP	SNV	664	664	.	+	.	ID=254;Variant_seq=G;Dbxref=dbSNP_129:rs53899372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399471.1	dbSNP	SNV	665	665	.	+	.	ID=255;Variant_seq=A;Dbxref=dbSNP_129:rs53938605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399471.1	dbSNP	SNV	666	666	.	+	.	ID=256;Variant_seq=A;Dbxref=dbSNP_129:rs53312572;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	677	677	.	+	.	ID=257;Variant_seq=C;Dbxref=dbSNP_129:rs53647626;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399471.1	dbSNP	SNV	678	678	.	+	.	ID=258;Variant_seq=A;Dbxref=dbSNP_129:rs53739890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	690	690	.	+	.	ID=259;Variant_seq=G;Dbxref=dbSNP_129:rs53418808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399471.1	dbSNP	SNV	692	692	.	+	.	ID=260;Variant_seq=A;Dbxref=dbSNP_129:rs54383599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	693	693	.	+	.	ID=261;Variant_seq=G;Dbxref=dbSNP_129:rs52958936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399471.1	dbSNP	SNV	2553	2553	.	+	.	ID=262;Variant_seq=A;Dbxref=dbSNP_129:rs21506500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399471.1	dbSNP	SNV	2735	2735	.	+	.	ID=263;Variant_seq=G;Dbxref=dbSNP_129:rs54369233;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399471.1	dbSNP	SNV	2785	2785	.	+	.	ID=264;Variant_seq=G;Dbxref=dbSNP_129:rs53632026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399471.1	dbSNP	SNV	3338	3338	.	+	.	ID=265;Variant_seq=T;Dbxref=dbSNP_129:rs53799992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037645.1	dbSNP	deletion	191	191	.	+	.	ID=266;Variant_seq=-;Dbxref=dbSNP_129:rs54178956;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037645.1	dbSNP	SNV	1904	1904	.	+	.	ID=267;Variant_seq=G;Dbxref=dbSNP_129:rs18517797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037645.1	dbSNP	SNV	1967	1967	.	+	.	ID=268;Variant_seq=T;Dbxref=dbSNP_129:rs18517716;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037645.1	dbSNP	SNV	1978	1978	.	+	.	ID=269;Variant_seq=C;Dbxref=dbSNP_129:rs18517689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037645.1	dbSNP	SNV	1981	1981	.	+	.	ID=270;Variant_seq=C;Dbxref=dbSNP_129:rs18517680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037645.1	dbSNP	SNV	1982	1982	.	+	.	ID=271;Variant_seq=A;Dbxref=dbSNP_129:rs18517671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037645.1	dbSNP	SNV	2966	2966	.	+	.	ID=272;Variant_seq=A;Dbxref=dbSNP_129:rs54298645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037645.1	dbSNP	SNV	2979	2979	.	+	.	ID=273;Variant_seq=A;Dbxref=dbSNP_129:rs53748013;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037645.1	dbSNP	SNV	8466	8466	.	+	.	ID=274;Variant_seq=C;Dbxref=dbSNP_129:rs53810545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398568.1	dbSNP	SNV	7717	7717	.	+	.	ID=275;Variant_seq=A;Dbxref=dbSNP_129:rs20292794;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398568.1	dbSNP	SNV	7730	7730	.	+	.	ID=276;Variant_seq=T;Dbxref=dbSNP_129:rs21478381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398568.1	dbSNP	SNV	9887	9887	.	+	.	ID=277;Variant_seq=G;Dbxref=dbSNP_129:rs20573227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398568.1	dbSNP	SNV	10445	10445	.	+	.	ID=278;Variant_seq=T;Dbxref=dbSNP_129:rs54300740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398568.1	dbSNP	SNV	10827	10827	.	+	.	ID=279;Variant_seq=T;Dbxref=dbSNP_129:rs20293122;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398457.1	dbSNP	SNV	381	381	.	+	.	ID=280;Variant_seq=C;Dbxref=dbSNP_129:rs53431051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398457.1	dbSNP	SNV	460	460	.	+	.	ID=281;Variant_seq=A;Dbxref=dbSNP_129:rs53966042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398457.1	dbSNP	SNV	462	462	.	+	.	ID=282;Variant_seq=G;Dbxref=dbSNP_129:rs54133790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	465	465	.	+	.	ID=283;Variant_seq=T;Dbxref=dbSNP_129:rs53321329;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	471	471	.	+	.	ID=284;Variant_seq=G;Dbxref=dbSNP_129:rs54251911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	480	480	.	+	.	ID=285;Variant_seq=T;Dbxref=dbSNP_129:rs52879113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	483	483	.	+	.	ID=286;Variant_seq=T;Dbxref=dbSNP_129:rs53064643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398457.1	dbSNP	SNV	485	485	.	+	.	ID=287;Variant_seq=T;Dbxref=dbSNP_129:rs53212544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398457.1	dbSNP	SNV	493	493	.	+	.	ID=288;Variant_seq=T;Dbxref=dbSNP_129:rs53781526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	497	497	.	+	.	ID=289;Variant_seq=A;Dbxref=dbSNP_129:rs54388998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398457.1	dbSNP	SNV	505	505	.	+	.	ID=290;Variant_seq=A;Dbxref=dbSNP_129:rs53023667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398457.1	dbSNP	SNV	511	511	.	+	.	ID=291;Variant_seq=C;Dbxref=dbSNP_129:rs53653778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398457.1	dbSNP	SNV	528	528	.	+	.	ID=292;Variant_seq=T;Dbxref=dbSNP_129:rs53480326;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398457.1	dbSNP	SNV	529	529	.	+	.	ID=293;Variant_seq=A;Dbxref=dbSNP_129:rs54267192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398457.1	dbSNP	SNV	538	538	.	+	.	ID=294;Variant_seq=G;Dbxref=dbSNP_129:rs53328546;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399071.1	dbSNP	SNV	298	298	.	+	.	ID=295;Variant_seq=T;Dbxref=dbSNP_129:rs53987119;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399071.1	dbSNP	SNV	303	303	.	+	.	ID=296;Variant_seq=T;Dbxref=dbSNP_129:rs54110239;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399071.1	dbSNP	SNV	307	307	.	+	.	ID=297;Variant_seq=C;Dbxref=dbSNP_129:rs53229403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399071.1	dbSNP	SNV	319	319	.	+	.	ID=298;Variant_seq=C;Dbxref=dbSNP_129:rs54218630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399071.1	dbSNP	SNV	326	326	.	+	.	ID=299;Variant_seq=T;Dbxref=dbSNP_129:rs53556185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399071.1	dbSNP	SNV	330	330	.	+	.	ID=300;Variant_seq=C;Dbxref=dbSNP_129:rs53314766;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398946.1	dbSNP	SNV	5270	5270	.	+	.	ID=301;Variant_seq=C;Dbxref=dbSNP_129:rs54297065;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398946.1	dbSNP	SNV	6322	6322	.	+	.	ID=302;Variant_seq=T;Dbxref=dbSNP_129:rs21026919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398736.1	dbSNP	SNV	6603	6603	.	+	.	ID=303;Variant_seq=G;Dbxref=dbSNP_129:rs20192427;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399741.1	dbSNP	SNV	1643	1643	.	+	.	ID=304;Variant_seq=T;Dbxref=dbSNP_129:rs53634523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399741.1	dbSNP	SNV	1648	1648	.	+	.	ID=305;Variant_seq=T;Dbxref=dbSNP_129:rs53349443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399741.1	dbSNP	SNV	1651	1651	.	+	.	ID=306;Variant_seq=T;Dbxref=dbSNP_129:rs54005014;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399741.1	dbSNP	insertion	1651	1651	.	+	.	ID=307;Variant_seq=TT;Dbxref=dbSNP_129:rs53010902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH399741.1	dbSNP	SNV	3850	3850	.	+	.	ID=308;Variant_seq=A;Dbxref=dbSNP_129:rs19532668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399741.1	dbSNP	SNV	3862	3862	.	+	.	ID=309;Variant_seq=C;Dbxref=dbSNP_129:rs19532658;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399741.1	dbSNP	SNV	3872	3872	.	+	.	ID=310;Variant_seq=G;Dbxref=dbSNP_129:rs19532648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399741.1	dbSNP	SNV	3874	3874	.	+	.	ID=311;Variant_seq=T;Dbxref=dbSNP_129:rs19532638;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399741.1	dbSNP	SNV	3876	3876	.	+	.	ID=312;Variant_seq=C;Dbxref=dbSNP_129:rs19532628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399741.1	dbSNP	SNV	3881	3881	.	+	.	ID=313;Variant_seq=A;Dbxref=dbSNP_129:rs19532618;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399741.1	dbSNP	SNV	3885	3885	.	+	.	ID=314;Variant_seq=G;Dbxref=dbSNP_129:rs19532608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399741.1	dbSNP	SNV	3887	3887	.	+	.	ID=315;Variant_seq=G;Dbxref=dbSNP_129:rs19532598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399741.1	dbSNP	SNV	3899	3899	.	+	.	ID=316;Variant_seq=C;Dbxref=dbSNP_129:rs19532578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399741.1	dbSNP	SNV	3900	3900	.	+	.	ID=317;Variant_seq=T;Dbxref=dbSNP_129:rs19532568;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040195.1	dbSNP	SNV	962	962	.	+	.	ID=318;Variant_seq=C;Dbxref=dbSNP_129:rs54192325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040195.1	dbSNP	SNV	987	987	.	+	.	ID=319;Variant_seq=T;Dbxref=dbSNP_129:rs53396464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040195.1	dbSNP	SNV	993	993	.	+	.	ID=320;Variant_seq=C;Dbxref=dbSNP_129:rs54026267;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040195.1	dbSNP	SNV	1002	1002	.	+	.	ID=321;Variant_seq=A;Dbxref=dbSNP_129:rs53433461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040195.1	dbSNP	SNV	5077	5077	.	+	.	ID=322;Variant_seq=C;Dbxref=dbSNP_129:rs20037367;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040195.1	dbSNP	SNV	5078	5078	.	+	.	ID=323;Variant_seq=T;Dbxref=dbSNP_129:rs20037377;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400456.1	dbSNP	SNV	1694	1694	.	+	.	ID=324;Variant_seq=C;Dbxref=dbSNP_129:rs18530276;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400456.1	dbSNP	SNV	1739	1739	.	+	.	ID=325;Variant_seq=A;Dbxref=dbSNP_129:rs18530285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400456.1	dbSNP	SNV	1753	1753	.	+	.	ID=326;Variant_seq=T;Dbxref=dbSNP_129:rs18530294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400456.1	dbSNP	SNV	2559	2559	.	+	.	ID=327;Variant_seq=A;Dbxref=dbSNP_129:rs54088873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400456.1	dbSNP	SNV	2876	2876	.	+	.	ID=328;Variant_seq=A;Dbxref=dbSNP_129:rs53347912;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400456.1	dbSNP	SNV	2892	2892	.	+	.	ID=329;Variant_seq=G;Dbxref=dbSNP_129:rs21676621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042272.1	dbSNP	SNV	47	47	.	+	.	ID=330;Variant_seq=T;Dbxref=dbSNP_129:rs18289950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042272.1	dbSNP	SNV	286	286	.	+	.	ID=331;Variant_seq=T;Dbxref=dbSNP_129:rs18289968;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042272.1	dbSNP	SNV	291	291	.	+	.	ID=332;Variant_seq=T;Dbxref=dbSNP_129:rs18289977;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042272.1	dbSNP	SNV	394	394	.	+	.	ID=333;Variant_seq=G;Dbxref=dbSNP_129:rs18289986;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042272.1	dbSNP	SNV	404	404	.	+	.	ID=334;Variant_seq=A;Dbxref=dbSNP_129:rs18289995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042272.1	dbSNP	SNV	559	559	.	+	.	ID=335;Variant_seq=A;Dbxref=dbSNP_129:rs54370913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042272.1	dbSNP	SNV	572	572	.	+	.	ID=336;Variant_seq=A;Dbxref=dbSNP_129:rs53996082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042272.1	dbSNP	SNV	576	576	.	+	.	ID=337;Variant_seq=T;Dbxref=dbSNP_129:rs53760294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042272.1	dbSNP	SNV	577	577	.	+	.	ID=338;Variant_seq=T;Dbxref=dbSNP_129:rs53119248;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042272.1	dbSNP	SNV	588	588	.	+	.	ID=339;Variant_seq=T;Dbxref=dbSNP_129:rs54203438;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042272.1	dbSNP	SNV	1606	1606	.	+	.	ID=340;Variant_seq=T;Dbxref=dbSNP_129:rs53869861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400527.1	dbSNP	SNV	102	102	.	+	.	ID=341;Variant_seq=G;Dbxref=dbSNP_129:rs54142521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400527.1	dbSNP	SNV	140	140	.	+	.	ID=342;Variant_seq=T;Dbxref=dbSNP_129:rs53110296;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400527.1	dbSNP	SNV	141	141	.	+	.	ID=343;Variant_seq=G;Dbxref=dbSNP_129:rs53832430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038539.1	dbSNP	SNV	5127	5127	.	+	.	ID=344;Variant_seq=C;Dbxref=dbSNP_129:rs52951640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038539.1	dbSNP	SNV	5129	5129	.	+	.	ID=345;Variant_seq=C;Dbxref=dbSNP_129:rs54048880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038539.1	dbSNP	SNV	5138	5138	.	+	.	ID=346;Variant_seq=C;Dbxref=dbSNP_129:rs54393102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038539.1	dbSNP	SNV	5148	5148	.	+	.	ID=347;Variant_seq=T;Dbxref=dbSNP_129:rs54137527;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038539.1	dbSNP	SNV	5157	5157	.	+	.	ID=348;Variant_seq=T;Dbxref=dbSNP_129:rs53161120;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	240	240	.	+	.	ID=349;Variant_seq=T;Dbxref=dbSNP_129:rs19620893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	254	254	.	+	.	ID=350;Variant_seq=T;Dbxref=dbSNP_129:rs54316437;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	337	337	.	+	.	ID=351;Variant_seq=C;Dbxref=dbSNP_129:rs53710806;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046464.1	dbSNP	SNV	352	352	.	+	.	ID=352;Variant_seq=C;Dbxref=dbSNP_129:rs53423664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	356	356	.	+	.	ID=353;Variant_seq=T;Dbxref=dbSNP_129:rs53534713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	deletion	360	360	.	+	.	ID=354;Variant_seq=-;Dbxref=dbSNP_129:rs53642322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	406	406	.	+	.	ID=355;Variant_seq=C;Dbxref=dbSNP_129:rs53591616;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1493	1493	.	+	.	ID=356;Variant_seq=C;Dbxref=dbSNP_129:rs53290854;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1495	1495	.	+	.	ID=357;Variant_seq=A;Dbxref=dbSNP_129:rs53040346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1499	1499	.	+	.	ID=358;Variant_seq=T;Dbxref=dbSNP_129:rs52900040;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1517	1517	.	+	.	ID=359;Variant_seq=T;Dbxref=dbSNP_129:rs53446067;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1526	1526	.	+	.	ID=360;Variant_seq=G;Dbxref=dbSNP_129:rs53710148;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1555	1555	.	+	.	ID=361;Variant_seq=A;Dbxref=dbSNP_129:rs53891519;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1569	1569	.	+	.	ID=362;Variant_seq=C;Dbxref=dbSNP_129:rs53909569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046464.1	dbSNP	SNV	1580	1580	.	+	.	ID=363;Variant_seq=T;Dbxref=dbSNP_129:rs53017853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1602	1602	.	+	.	ID=364;Variant_seq=C;Dbxref=dbSNP_129:rs52867304;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	deletion	1612	1612	.	+	.	ID=365;Variant_seq=-;Dbxref=dbSNP_129:rs53059957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1613	1613	.	+	.	ID=366;Variant_seq=C;Dbxref=dbSNP_129:rs53704135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1615	1615	.	+	.	ID=367;Variant_seq=A;Dbxref=dbSNP_129:rs52957826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1616	1616	.	+	.	ID=368;Variant_seq=C;Dbxref=dbSNP_129:rs52905499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1623	1623	.	+	.	ID=369;Variant_seq=A;Dbxref=dbSNP_129:rs53887701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1624	1624	.	+	.	ID=370;Variant_seq=T;Dbxref=dbSNP_129:rs53780243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1629	1629	.	+	.	ID=371;Variant_seq=T;Dbxref=dbSNP_129:rs54110431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046464.1	dbSNP	SNV	1636	1636	.	+	.	ID=372;Variant_seq=C;Dbxref=dbSNP_129:rs53345818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1637	1637	.	+	.	ID=373;Variant_seq=A;Dbxref=dbSNP_129:rs53075016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1651	1651	.	+	.	ID=374;Variant_seq=G;Dbxref=dbSNP_129:rs54009685;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1656	1656	.	+	.	ID=375;Variant_seq=T;Dbxref=dbSNP_129:rs53675237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1688	1688	.	+	.	ID=376;Variant_seq=A;Dbxref=dbSNP_129:rs54171744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1704	1704	.	+	.	ID=377;Variant_seq=T;Dbxref=dbSNP_129:rs53468055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1710	1710	.	+	.	ID=378;Variant_seq=T;Dbxref=dbSNP_129:rs54159285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1722	1722	.	+	.	ID=379;Variant_seq=A;Dbxref=dbSNP_129:rs52939737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046464.1	dbSNP	SNV	1730	1730	.	+	.	ID=380;Variant_seq=T;Dbxref=dbSNP_129:rs52903088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046464.1	dbSNP	SNV	1731	1731	.	+	.	ID=381;Variant_seq=T;Dbxref=dbSNP_129:rs54202429;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1735	1735	.	+	.	ID=382;Variant_seq=C;Dbxref=dbSNP_129:rs53848205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046464.1	dbSNP	SNV	1739	1739	.	+	.	ID=383;Variant_seq=G;Dbxref=dbSNP_129:rs54012730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046296.1	dbSNP	SNV	1120	1120	.	+	.	ID=384;Variant_seq=A;Dbxref=dbSNP_129:rs20833336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041769.1	dbSNP	SNV	1692	1692	.	+	.	ID=385;Variant_seq=A;Dbxref=dbSNP_129:rs54272981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041769.1	dbSNP	SNV	1693	1693	.	+	.	ID=386;Variant_seq=T;Dbxref=dbSNP_129:rs54190000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041769.1	dbSNP	SNV	1696	1696	.	+	.	ID=387;Variant_seq=T;Dbxref=dbSNP_129:rs52947741;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041769.1	dbSNP	SNV	1697	1697	.	+	.	ID=388;Variant_seq=A;Dbxref=dbSNP_129:rs53798936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041769.1	dbSNP	SNV	1698	1698	.	+	.	ID=389;Variant_seq=A;Dbxref=dbSNP_129:rs53405402;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398927.1	dbSNP	SNV	2441	2441	.	+	.	ID=390;Variant_seq=C;Dbxref=dbSNP_129:rs20150574;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399034.1	dbSNP	SNV	1766	1766	.	+	.	ID=391;Variant_seq=G;Dbxref=dbSNP_129:rs21424465;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040278.1	dbSNP	SNV	3743	3743	.	+	.	ID=392;Variant_seq=T;Dbxref=dbSNP_129:rs19039036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043927.1	dbSNP	SNV	598	598	.	+	.	ID=393;Variant_seq=C;Dbxref=dbSNP_129:rs53138713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400499.1	dbSNP	SNV	1455	1455	.	+	.	ID=394;Variant_seq=A;Dbxref=dbSNP_129:rs21104595;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400499.1	dbSNP	SNV	1488	1488	.	+	.	ID=395;Variant_seq=A;Dbxref=dbSNP_129:rs21104615;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400499.1	dbSNP	SNV	2240	2240	.	+	.	ID=396;Variant_seq=G;Dbxref=dbSNP_129:rs21105834;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041491.1	dbSNP	SNV	1013	1013	.	+	.	ID=397;Variant_seq=A;Dbxref=dbSNP_129:rs19489175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044356.1	dbSNP	SNV	921	921	.	+	.	ID=398;Variant_seq=A;Dbxref=dbSNP_129:rs54339687;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044356.1	dbSNP	SNV	926	926	.	+	.	ID=399;Variant_seq=A;Dbxref=dbSNP_129:rs53294790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044356.1	dbSNP	SNV	930	930	.	+	.	ID=400;Variant_seq=C;Dbxref=dbSNP_129:rs54065206;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047816.1	dbSNP	SNV	99	99	.	+	.	ID=401;Variant_seq=T;Dbxref=dbSNP_129:rs19850922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047816.1	dbSNP	SNV	121	121	.	+	.	ID=402;Variant_seq=G;Dbxref=dbSNP_129:rs19850932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040632.1	dbSNP	SNV	2018	2018	.	+	.	ID=403;Variant_seq=T;Dbxref=dbSNP_129:rs18423753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040632.1	dbSNP	SNV	3610	3610	.	+	.	ID=404;Variant_seq=G;Dbxref=dbSNP_129:rs18929413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040632.1	dbSNP	SNV	4378	4378	.	+	.	ID=405;Variant_seq=G;Dbxref=dbSNP_129:rs20223151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044751.1	dbSNP	SNV	951	951	.	+	.	ID=406;Variant_seq=T;Dbxref=dbSNP_129:rs20900415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044751.1	dbSNP	SNV	2892	2892	.	+	.	ID=407;Variant_seq=C;Dbxref=dbSNP_129:rs19414506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400079.1	dbSNP	SNV	587	587	.	+	.	ID=408;Variant_seq=C;Dbxref=dbSNP_129:rs21561684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400079.1	dbSNP	SNV	600	600	.	+	.	ID=409;Variant_seq=T;Dbxref=dbSNP_129:rs21561694;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400079.1	dbSNP	SNV	602	602	.	+	.	ID=410;Variant_seq=A;Dbxref=dbSNP_129:rs21561704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043549.1	dbSNP	SNV	207	207	.	+	.	ID=411;Variant_seq=A;Dbxref=dbSNP_129:rs20350081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043549.1	dbSNP	SNV	1552	1552	.	+	.	ID=412;Variant_seq=A;Dbxref=dbSNP_129:rs21688254;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043549.1	dbSNP	SNV	1862	1862	.	+	.	ID=413;Variant_seq=A;Dbxref=dbSNP_129:rs21688200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043549.1	dbSNP	SNV	2383	2383	.	+	.	ID=414;Variant_seq=T;Dbxref=dbSNP_129:rs21688020;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043549.1	dbSNP	SNV	2618	2618	.	+	.	ID=415;Variant_seq=T;Dbxref=dbSNP_129:rs21687975;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043549.1	dbSNP	SNV	2793	2793	.	+	.	ID=416;Variant_seq=C;Dbxref=dbSNP_129:rs21687939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043549.1	dbSNP	insertion	2925	2925	.	+	.	ID=417;Variant_seq=AAAGATG;Dbxref=dbSNP_129:rs53611127;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02043549.1	dbSNP	SNV	3113	3113	.	+	.	ID=418;Variant_seq=C;Dbxref=dbSNP_129:rs21687930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043549.1	dbSNP	SNV	3202	3202	.	+	.	ID=419;Variant_seq=A;Dbxref=dbSNP_129:rs21687921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044379.1	dbSNP	SNV	2481	2481	.	+	.	ID=420;Variant_seq=A;Dbxref=dbSNP_129:rs19552781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044379.1	dbSNP	SNV	2482	2482	.	+	.	ID=421;Variant_seq=G;Dbxref=dbSNP_129:rs19552791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044379.1	dbSNP	SNV	2492	2492	.	+	.	ID=422;Variant_seq=G;Dbxref=dbSNP_129:rs19552811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044379.1	dbSNP	SNV	2493	2493	.	+	.	ID=423;Variant_seq=T;Dbxref=dbSNP_129:rs19552821;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044379.1	dbSNP	SNV	2497	2497	.	+	.	ID=424;Variant_seq=A;Dbxref=dbSNP_129:rs19552831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044379.1	dbSNP	SNV	2500	2500	.	+	.	ID=425;Variant_seq=A;Dbxref=dbSNP_129:rs19552841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044379.1	dbSNP	SNV	2504	2504	.	+	.	ID=426;Variant_seq=T;Dbxref=dbSNP_129:rs19552851;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044379.1	dbSNP	SNV	2505	2505	.	+	.	ID=427;Variant_seq=A;Dbxref=dbSNP_129:rs19552861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398871.1	dbSNP	SNV	1648	1648	.	+	.	ID=428;Variant_seq=A;Dbxref=dbSNP_129:rs18173421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398871.1	dbSNP	SNV	5640	5640	.	+	.	ID=429;Variant_seq=G;Dbxref=dbSNP_129:rs19931150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398871.1	dbSNP	SNV	6186	6186	.	+	.	ID=430;Variant_seq=T;Dbxref=dbSNP_129:rs54179884;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398871.1	dbSNP	SNV	6557	6557	.	+	.	ID=431;Variant_seq=G;Dbxref=dbSNP_129:rs53372340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398871.1	dbSNP	SNV	8375	8375	.	+	.	ID=432;Variant_seq=A;Dbxref=dbSNP_129:rs53540638;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400914.1	dbSNP	SNV	945	945	.	+	.	ID=433;Variant_seq=T;Dbxref=dbSNP_129:rs18038896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400914.1	dbSNP	SNV	963	963	.	+	.	ID=434;Variant_seq=G;Dbxref=dbSNP_129:rs18038869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400914.1	dbSNP	SNV	978	978	.	+	.	ID=435;Variant_seq=A;Dbxref=dbSNP_129:rs18038833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400914.1	dbSNP	SNV	993	993	.	+	.	ID=436;Variant_seq=T;Dbxref=dbSNP_129:rs18038815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400914.1	dbSNP	SNV	994	994	.	+	.	ID=437;Variant_seq=C;Dbxref=dbSNP_129:rs17889559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039133.1	dbSNP	SNV	242	242	.	+	.	ID=438;Variant_seq=C;Dbxref=dbSNP_129:rs20698793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039133.1	dbSNP	SNV	1432	1432	.	+	.	ID=439;Variant_seq=C;Dbxref=dbSNP_129:rs52909525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045589.1	dbSNP	SNV	1752	1752	.	+	.	ID=440;Variant_seq=A;Dbxref=dbSNP_129:rs21310922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045589.1	dbSNP	insertion	2128	2128	.	+	.	ID=441;Variant_seq=ACATGGGTAGTACATGATTA;Dbxref=dbSNP_129:rs53665302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02045589.1	dbSNP	SNV	2560	2560	.	+	.	ID=442;Variant_seq=C;Dbxref=dbSNP_129:rs53311244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045589.1	dbSNP	SNV	2657	2657	.	+	.	ID=443;Variant_seq=C;Dbxref=dbSNP_129:rs53411610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039455.1	dbSNP	SNV	1200	1200	.	+	.	ID=444;Variant_seq=G;Dbxref=dbSNP_129:rs18765656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039455.1	dbSNP	SNV	2872	2872	.	+	.	ID=445;Variant_seq=A;Dbxref=dbSNP_129:rs20865743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039618.1	dbSNP	SNV	966	966	.	+	.	ID=446;Variant_seq=C;Dbxref=dbSNP_129:rs53399109;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039618.1	dbSNP	SNV	972	972	.	+	.	ID=447;Variant_seq=C;Dbxref=dbSNP_129:rs53539870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039618.1	dbSNP	SNV	1008	1008	.	+	.	ID=448;Variant_seq=T;Dbxref=dbSNP_129:rs54136614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043527.1	dbSNP	SNV	640	640	.	+	.	ID=449;Variant_seq=T;Dbxref=dbSNP_129:rs53833384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398864.1	dbSNP	SNV	7370	7370	.	+	.	ID=450;Variant_seq=T;Dbxref=dbSNP_129:rs19831253;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398864.1	dbSNP	SNV	7448	7448	.	+	.	ID=451;Variant_seq=G;Dbxref=dbSNP_129:rs19831273;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8064	8064	.	+	.	ID=452;Variant_seq=A;Dbxref=dbSNP_129:rs19878309;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8440	8440	.	+	.	ID=453;Variant_seq=A;Dbxref=dbSNP_129:rs19878349;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8843	8843	.	+	.	ID=454;Variant_seq=A;Dbxref=dbSNP_129:rs53238794;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398864.1	dbSNP	SNV	8847	8847	.	+	.	ID=455;Variant_seq=G;Dbxref=dbSNP_129:rs53941557;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8862	8862	.	+	.	ID=456;Variant_seq=C;Dbxref=dbSNP_129:rs53242563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398864.1	dbSNP	SNV	8866	8866	.	+	.	ID=457;Variant_seq=A;Dbxref=dbSNP_129:rs53825426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8871	8871	.	+	.	ID=458;Variant_seq=G;Dbxref=dbSNP_129:rs53091027;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8900	8900	.	+	.	ID=459;Variant_seq=A;Dbxref=dbSNP_129:rs52891463;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8903	8903	.	+	.	ID=460;Variant_seq=A;Dbxref=dbSNP_129:rs54221431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398864.1	dbSNP	SNV	8909	8909	.	+	.	ID=461;Variant_seq=G;Dbxref=dbSNP_129:rs53326576;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8911	8911	.	+	.	ID=462;Variant_seq=A;Dbxref=dbSNP_129:rs53877931;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8920	8920	.	+	.	ID=463;Variant_seq=C;Dbxref=dbSNP_129:rs53815669;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398864.1	dbSNP	SNV	8921	8921	.	+	.	ID=464;Variant_seq=A;Dbxref=dbSNP_129:rs53450684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398864.1	dbSNP	SNV	8932	8932	.	+	.	ID=465;Variant_seq=T;Dbxref=dbSNP_129:rs54225153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398864.1	dbSNP	SNV	8940	8940	.	+	.	ID=466;Variant_seq=C;Dbxref=dbSNP_129:rs53128370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398864.1	dbSNP	SNV	8941	8941	.	+	.	ID=467;Variant_seq=G;Dbxref=dbSNP_129:rs54217152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8944	8944	.	+	.	ID=468;Variant_seq=G;Dbxref=dbSNP_129:rs53127769;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398864.1	dbSNP	SNV	8952	8952	.	+	.	ID=469;Variant_seq=A;Dbxref=dbSNP_129:rs54286896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040604.1	dbSNP	SNV	599	599	.	+	.	ID=470;Variant_seq=A;Dbxref=dbSNP_129:rs52969807;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040604.1	dbSNP	SNV	2324	2324	.	+	.	ID=471;Variant_seq=C;Dbxref=dbSNP_129:rs19040826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040604.1	dbSNP	SNV	3825	3825	.	+	.	ID=472;Variant_seq=C;Dbxref=dbSNP_129:rs20170251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036459.1	dbSNP	SNV	3458	3458	.	+	.	ID=473;Variant_seq=G;Dbxref=dbSNP_129:rs18777701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036459.1	dbSNP	SNV	3645	3645	.	+	.	ID=474;Variant_seq=G;Dbxref=dbSNP_129:rs53293628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036459.1	dbSNP	SNV	3662	3662	.	+	.	ID=475;Variant_seq=G;Dbxref=dbSNP_129:rs54378630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036459.1	dbSNP	SNV	5890	5890	.	+	.	ID=476;Variant_seq=A;Dbxref=dbSNP_129:rs21434906;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036459.1	dbSNP	SNV	8537	8537	.	+	.	ID=477;Variant_seq=A;Dbxref=dbSNP_129:rs19890845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036459.1	dbSNP	SNV	8688	8688	.	+	.	ID=478;Variant_seq=G;Dbxref=dbSNP_129:rs18026018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036459.1	dbSNP	SNV	8693	8693	.	+	.	ID=479;Variant_seq=A;Dbxref=dbSNP_129:rs18026045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036459.1	dbSNP	SNV	8697	8697	.	+	.	ID=480;Variant_seq=A;Dbxref=dbSNP_129:rs18026054;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036459.1	dbSNP	SNV	8698	8698	.	+	.	ID=481;Variant_seq=A;Dbxref=dbSNP_129:rs18026063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036459.1	dbSNP	SNV	8703	8703	.	+	.	ID=482;Variant_seq=A;Dbxref=dbSNP_129:rs18026081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036459.1	dbSNP	SNV	8712	8712	.	+	.	ID=483;Variant_seq=T;Dbxref=dbSNP_129:rs18026108;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036459.1	dbSNP	SNV	9618	9618	.	+	.	ID=484;Variant_seq=C;Dbxref=dbSNP_129:rs53574679;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036459.1	dbSNP	SNV	9621	9621	.	+	.	ID=485;Variant_seq=T;Dbxref=dbSNP_129:rs53714067;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036459.1	dbSNP	SNV	9627	9627	.	+	.	ID=486;Variant_seq=A;Dbxref=dbSNP_129:rs53808518;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049560.1	dbSNP	SNV	431	431	.	+	.	ID=487;Variant_seq=A;Dbxref=dbSNP_129:rs19546521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049560.1	dbSNP	SNV	446	446	.	+	.	ID=488;Variant_seq=C;Dbxref=dbSNP_129:rs19546531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049560.1	dbSNP	SNV	1431	1431	.	+	.	ID=489;Variant_seq=T;Dbxref=dbSNP_129:rs20946597;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400084.1	dbSNP	SNV	628	628	.	+	.	ID=490;Variant_seq=C;Dbxref=dbSNP_129:rs21249762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400084.1	dbSNP	SNV	1387	1387	.	+	.	ID=491;Variant_seq=C;Dbxref=dbSNP_129:rs53475935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400084.1	dbSNP	SNV	1460	1460	.	+	.	ID=492;Variant_seq=A;Dbxref=dbSNP_129:rs53934700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400084.1	dbSNP	SNV	1472	1472	.	+	.	ID=493;Variant_seq=C;Dbxref=dbSNP_129:rs54254644;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400084.1	dbSNP	SNV	1544	1544	.	+	.	ID=494;Variant_seq=G;Dbxref=dbSNP_129:rs53279053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400084.1	dbSNP	SNV	1583	1583	.	+	.	ID=495;Variant_seq=G;Dbxref=dbSNP_129:rs53704865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035981.1	dbSNP	SNV	10319	10319	.	+	.	ID=496;Variant_seq=A;Dbxref=dbSNP_129:rs20178457;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035981.1	dbSNP	SNV	22033	22033	.	+	.	ID=497;Variant_seq=C;Dbxref=dbSNP_129:rs19128672;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035981.1	dbSNP	SNV	22044	22044	.	+	.	ID=498;Variant_seq=A;Dbxref=dbSNP_129:rs19128602;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035981.1	dbSNP	SNV	22566	22566	.	+	.	ID=499;Variant_seq=G;Dbxref=dbSNP_129:rs54176901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035981.1	dbSNP	SNV	22572	22572	.	+	.	ID=500;Variant_seq=T;Dbxref=dbSNP_129:rs53397995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035981.1	dbSNP	SNV	22575	22575	.	+	.	ID=501;Variant_seq=T;Dbxref=dbSNP_129:rs53759887;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035981.1	dbSNP	SNV	22601	22601	.	+	.	ID=502;Variant_seq=T;Dbxref=dbSNP_129:rs52864049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035981.1	dbSNP	SNV	23125	23125	.	+	.	ID=503;Variant_seq=T;Dbxref=dbSNP_129:rs18419732;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399705.1	dbSNP	SNV	144	144	.	+	.	ID=504;Variant_seq=C;Dbxref=dbSNP_129:rs20340544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399705.1	dbSNP	SNV	155	155	.	+	.	ID=505;Variant_seq=A;Dbxref=dbSNP_129:rs20340564;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399705.1	dbSNP	SNV	1867	1867	.	+	.	ID=506;Variant_seq=A;Dbxref=dbSNP_129:rs20003436;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399705.1	dbSNP	SNV	2243	2243	.	+	.	ID=507;Variant_seq=A;Dbxref=dbSNP_129:rs53542784;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399705.1	dbSNP	SNV	3046	3046	.	+	.	ID=508;Variant_seq=T;Dbxref=dbSNP_129:rs21193710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	SNV	656	656	.	+	.	ID=509;Variant_seq=T;Dbxref=dbSNP_129:rs53346998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	SNV	657	657	.	+	.	ID=510;Variant_seq=A;Dbxref=dbSNP_129:rs52900167;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	SNV	659	659	.	+	.	ID=511;Variant_seq=T;Dbxref=dbSNP_129:rs53399550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398320.1	dbSNP	SNV	5325	5325	.	+	.	ID=512;Variant_seq=C;Dbxref=dbSNP_129:rs20257192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398320.1	dbSNP	SNV	5348	5348	.	+	.	ID=513;Variant_seq=A;Dbxref=dbSNP_129:rs20257172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	SNV	5400	5400	.	+	.	ID=514;Variant_seq=C;Dbxref=dbSNP_129:rs20257132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	SNV	7092	7092	.	+	.	ID=515;Variant_seq=G;Dbxref=dbSNP_129:rs21126834;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398320.1	dbSNP	SNV	7093	7093	.	+	.	ID=516;Variant_seq=C;Dbxref=dbSNP_129:rs21126824;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398320.1	dbSNP	SNV	7109	7109	.	+	.	ID=517;Variant_seq=A;Dbxref=dbSNP_129:rs21126794;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	SNV	7112	7112	.	+	.	ID=518;Variant_seq=C;Dbxref=dbSNP_129:rs21126784;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398320.1	dbSNP	SNV	8742	8742	.	+	.	ID=519;Variant_seq=A;Dbxref=dbSNP_129:rs20256982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	SNV	8883	8883	.	+	.	ID=520;Variant_seq=A;Dbxref=dbSNP_129:rs20256972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	SNV	9291	9291	.	+	.	ID=521;Variant_seq=A;Dbxref=dbSNP_129:rs20256932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	SNV	9700	9700	.	+	.	ID=522;Variant_seq=T;Dbxref=dbSNP_129:rs20256832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	SNV	9880	9880	.	+	.	ID=523;Variant_seq=A;Dbxref=dbSNP_129:rs20256772;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398320.1	dbSNP	insertion	10781	10781	.	+	.	ID=524;Variant_seq=CC;Dbxref=dbSNP_129:rs54221417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH398320.1	dbSNP	SNV	10782	10782	.	+	.	ID=525;Variant_seq=T;Dbxref=dbSNP_129:rs53948091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398320.1	dbSNP	insertion	10782	10782	.	+	.	ID=526;Variant_seq=TC;Dbxref=dbSNP_129:rs53304360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02041061.1	dbSNP	SNV	1293	1293	.	+	.	ID=527;Variant_seq=A;Dbxref=dbSNP_129:rs20946074;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	1402	1402	.	+	.	ID=528;Variant_seq=T;Dbxref=dbSNP_129:rs20945994;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1700	1700	.	+	.	ID=529;Variant_seq=T;Dbxref=dbSNP_129:rs20945734;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1705	1705	.	+	.	ID=530;Variant_seq=T;Dbxref=dbSNP_129:rs20945724;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1712	1712	.	+	.	ID=531;Variant_seq=T;Dbxref=dbSNP_129:rs20945714;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1716	1716	.	+	.	ID=532;Variant_seq=C;Dbxref=dbSNP_129:rs20945704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041061.1	dbSNP	SNV	1722	1722	.	+	.	ID=533;Variant_seq=T;Dbxref=dbSNP_129:rs20945693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1729	1729	.	+	.	ID=534;Variant_seq=T;Dbxref=dbSNP_129:rs20945683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1730	1730	.	+	.	ID=535;Variant_seq=A;Dbxref=dbSNP_129:rs20945673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	1738	1738	.	+	.	ID=536;Variant_seq=A;Dbxref=dbSNP_129:rs20945653;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	1742	1742	.	+	.	ID=537;Variant_seq=A;Dbxref=dbSNP_129:rs20945643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1743	1743	.	+	.	ID=538;Variant_seq=C;Dbxref=dbSNP_129:rs20945633;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041061.1	dbSNP	SNV	1744	1744	.	+	.	ID=539;Variant_seq=A;Dbxref=dbSNP_129:rs20945623;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	1745	1745	.	+	.	ID=540;Variant_seq=A;Dbxref=dbSNP_129:rs20945613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	1752	1752	.	+	.	ID=541;Variant_seq=T;Dbxref=dbSNP_129:rs20945593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1754	1754	.	+	.	ID=542;Variant_seq=T;Dbxref=dbSNP_129:rs20945583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	1768	1768	.	+	.	ID=543;Variant_seq=C;Dbxref=dbSNP_129:rs20945563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041061.1	dbSNP	SNV	1822	1822	.	+	.	ID=544;Variant_seq=C;Dbxref=dbSNP_129:rs19568906;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041061.1	dbSNP	SNV	2064	2064	.	+	.	ID=545;Variant_seq=C;Dbxref=dbSNP_129:rs20945062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041061.1	dbSNP	SNV	2067	2067	.	+	.	ID=546;Variant_seq=T;Dbxref=dbSNP_129:rs20945052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	2413	2413	.	+	.	ID=547;Variant_seq=A;Dbxref=dbSNP_129:rs53823827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041061.1	dbSNP	SNV	2415	2415	.	+	.	ID=548;Variant_seq=A;Dbxref=dbSNP_129:rs53839679;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041061.1	dbSNP	SNV	2660	2660	.	+	.	ID=549;Variant_seq=C;Dbxref=dbSNP_129:rs20944342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035672.1	dbSNP	SNV	1723	1723	.	+	.	ID=550;Variant_seq=C;Dbxref=dbSNP_129:rs53578337;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035672.1	dbSNP	SNV	4366	4366	.	+	.	ID=551;Variant_seq=A;Dbxref=dbSNP_129:rs54366503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035672.1	dbSNP	SNV	4755	4755	.	+	.	ID=552;Variant_seq=A;Dbxref=dbSNP_129:rs52875559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035672.1	dbSNP	SNV	5801	5801	.	+	.	ID=553;Variant_seq=A;Dbxref=dbSNP_129:rs20285985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035672.1	dbSNP	SNV	6115	6115	.	+	.	ID=554;Variant_seq=A;Dbxref=dbSNP_129:rs53140519;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035672.1	dbSNP	SNV	9107	9107	.	+	.	ID=555;Variant_seq=A;Dbxref=dbSNP_129:rs19355783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035672.1	dbSNP	SNV	12987	12987	.	+	.	ID=556;Variant_seq=A;Dbxref=dbSNP_129:rs19952413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042992.1	dbSNP	SNV	1067	1067	.	+	.	ID=557;Variant_seq=T;Dbxref=dbSNP_129:rs54045490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042992.1	dbSNP	SNV	1073	1073	.	+	.	ID=558;Variant_seq=T;Dbxref=dbSNP_129:rs53127197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042992.1	dbSNP	SNV	1223	1223	.	+	.	ID=559;Variant_seq=C;Dbxref=dbSNP_129:rs54284935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042992.1	dbSNP	SNV	1720	1720	.	+	.	ID=560;Variant_seq=A;Dbxref=dbSNP_129:rs19952569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042992.1	dbSNP	SNV	2367	2367	.	+	.	ID=561;Variant_seq=C;Dbxref=dbSNP_129:rs18026090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042992.1	dbSNP	SNV	2368	2368	.	+	.	ID=562;Variant_seq=C;Dbxref=dbSNP_129:rs18026099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042992.1	dbSNP	SNV	2373	2373	.	+	.	ID=563;Variant_seq=T;Dbxref=dbSNP_129:rs18026108;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042992.1	dbSNP	SNV	2379	2379	.	+	.	ID=564;Variant_seq=A;Dbxref=dbSNP_129:rs18026135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398701.1	dbSNP	SNV	339	339	.	+	.	ID=565;Variant_seq=T;Dbxref=dbSNP_129:rs19651559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398701.1	dbSNP	SNV	5957	5957	.	+	.	ID=566;Variant_seq=G;Dbxref=dbSNP_129:rs19651579;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399834.1	dbSNP	SNV	1309	1309	.	+	.	ID=567;Variant_seq=G;Dbxref=dbSNP_129:rs19850381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399834.1	dbSNP	SNV	1330	1330	.	+	.	ID=568;Variant_seq=C;Dbxref=dbSNP_129:rs19850361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399834.1	dbSNP	SNV	2010	2010	.	+	.	ID=569;Variant_seq=G;Dbxref=dbSNP_129:rs54175216;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399834.1	dbSNP	SNV	2358	2358	.	+	.	ID=570;Variant_seq=T;Dbxref=dbSNP_129:rs53461032;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399834.1	dbSNP	SNV	2721	2721	.	+	.	ID=571;Variant_seq=C;Dbxref=dbSNP_129:rs18900364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398408.1	dbSNP	SNV	56	56	.	+	.	ID=572;Variant_seq=G;Dbxref=dbSNP_129:rs21580793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398408.1	dbSNP	SNV	65	65	.	+	.	ID=573;Variant_seq=A;Dbxref=dbSNP_129:rs21580803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398408.1	dbSNP	SNV	166	166	.	+	.	ID=574;Variant_seq=T;Dbxref=dbSNP_129:rs21580823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398408.1	dbSNP	SNV	170	170	.	+	.	ID=575;Variant_seq=T;Dbxref=dbSNP_129:rs21580833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398408.1	dbSNP	SNV	288	288	.	+	.	ID=576;Variant_seq=A;Dbxref=dbSNP_129:rs21580853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398408.1	dbSNP	SNV	380	380	.	+	.	ID=577;Variant_seq=T;Dbxref=dbSNP_129:rs21580873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398408.1	dbSNP	SNV	456	456	.	+	.	ID=578;Variant_seq=C;Dbxref=dbSNP_129:rs21580883;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398408.1	dbSNP	SNV	8716	8716	.	+	.	ID=579;Variant_seq=A;Dbxref=dbSNP_129:rs53559084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398408.1	dbSNP	SNV	8723	8723	.	+	.	ID=580;Variant_seq=C;Dbxref=dbSNP_129:rs54364850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398408.1	dbSNP	SNV	8740	8740	.	+	.	ID=581;Variant_seq=T;Dbxref=dbSNP_129:rs53706476;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400179.1	dbSNP	deletion	777	779	.	+	.	ID=582;Variant_seq=-;Dbxref=dbSNP_129:rs53409412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=GGT
CH400179.1	dbSNP	SNV	785	785	.	+	.	ID=583;Variant_seq=T;Dbxref=dbSNP_129:rs53538184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400179.1	dbSNP	SNV	840	840	.	+	.	ID=584;Variant_seq=T;Dbxref=dbSNP_129:rs54358188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400179.1	dbSNP	SNV	1103	1103	.	+	.	ID=585;Variant_seq=T;Dbxref=dbSNP_129:rs53433913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400179.1	dbSNP	SNV	1115	1115	.	+	.	ID=586;Variant_seq=A;Dbxref=dbSNP_129:rs54277660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400179.1	dbSNP	SNV	1116	1116	.	+	.	ID=587;Variant_seq=C;Dbxref=dbSNP_129:rs53967174;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400179.1	dbSNP	SNV	1121	1121	.	+	.	ID=588;Variant_seq=T;Dbxref=dbSNP_129:rs53054243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400179.1	dbSNP	SNV	1132	1132	.	+	.	ID=589;Variant_seq=G;Dbxref=dbSNP_129:rs52925150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400179.1	dbSNP	SNV	1137	1137	.	+	.	ID=590;Variant_seq=G;Dbxref=dbSNP_129:rs53529413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400179.1	dbSNP	SNV	1212	1212	.	+	.	ID=591;Variant_seq=C;Dbxref=dbSNP_129:rs53878556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400179.1	dbSNP	SNV	2092	2092	.	+	.	ID=592;Variant_seq=A;Dbxref=dbSNP_129:rs54368331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400179.1	dbSNP	SNV	2096	2096	.	+	.	ID=593;Variant_seq=A;Dbxref=dbSNP_129:rs53891125;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1292	1292	.	+	.	ID=594;Variant_seq=T;Dbxref=dbSNP_129:rs21071101;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1694	1694	.	+	.	ID=595;Variant_seq=C;Dbxref=dbSNP_129:rs21069932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1709	1709	.	+	.	ID=596;Variant_seq=G;Dbxref=dbSNP_129:rs21069922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1711	1711	.	+	.	ID=597;Variant_seq=T;Dbxref=dbSNP_129:rs21069912;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1712	1712	.	+	.	ID=598;Variant_seq=A;Dbxref=dbSNP_129:rs21069902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1720	1720	.	+	.	ID=599;Variant_seq=T;Dbxref=dbSNP_129:rs21069892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1721	1721	.	+	.	ID=600;Variant_seq=C;Dbxref=dbSNP_129:rs21069882;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1724	1724	.	+	.	ID=601;Variant_seq=A;Dbxref=dbSNP_129:rs21069872;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1732	1732	.	+	.	ID=602;Variant_seq=G;Dbxref=dbSNP_129:rs21069852;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1733	1733	.	+	.	ID=603;Variant_seq=A;Dbxref=dbSNP_129:rs21069842;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1736	1736	.	+	.	ID=604;Variant_seq=C;Dbxref=dbSNP_129:rs21069822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1737	1737	.	+	.	ID=605;Variant_seq=T;Dbxref=dbSNP_129:rs21069812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1755	1755	.	+	.	ID=606;Variant_seq=G;Dbxref=dbSNP_129:rs21069742;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1773	1773	.	+	.	ID=607;Variant_seq=A;Dbxref=dbSNP_129:rs21069692;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1774	1774	.	+	.	ID=608;Variant_seq=A;Dbxref=dbSNP_129:rs21069682;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1775	1775	.	+	.	ID=609;Variant_seq=A;Dbxref=dbSNP_129:rs21069672;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1778	1778	.	+	.	ID=610;Variant_seq=T;Dbxref=dbSNP_129:rs21069662;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1785	1785	.	+	.	ID=611;Variant_seq=A;Dbxref=dbSNP_129:rs21069652;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1787	1787	.	+	.	ID=612;Variant_seq=C;Dbxref=dbSNP_129:rs21069642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1788	1788	.	+	.	ID=613;Variant_seq=A;Dbxref=dbSNP_129:rs21069631;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1793	1793	.	+	.	ID=614;Variant_seq=C;Dbxref=dbSNP_129:rs21069621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1811	1811	.	+	.	ID=615;Variant_seq=C;Dbxref=dbSNP_129:rs21069611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1812	1812	.	+	.	ID=616;Variant_seq=G;Dbxref=dbSNP_129:rs21069601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1820	1820	.	+	.	ID=617;Variant_seq=T;Dbxref=dbSNP_129:rs21069571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1823	1823	.	+	.	ID=618;Variant_seq=G;Dbxref=dbSNP_129:rs21069561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1824	1824	.	+	.	ID=619;Variant_seq=A;Dbxref=dbSNP_129:rs21069551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1829	1829	.	+	.	ID=620;Variant_seq=G;Dbxref=dbSNP_129:rs21069521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046439.1	dbSNP	SNV	1847	1847	.	+	.	ID=621;Variant_seq=A;Dbxref=dbSNP_129:rs21069511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1850	1850	.	+	.	ID=622;Variant_seq=T;Dbxref=dbSNP_129:rs21069501;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1852	1852	.	+	.	ID=623;Variant_seq=A;Dbxref=dbSNP_129:rs21069491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	1853	1853	.	+	.	ID=624;Variant_seq=C;Dbxref=dbSNP_129:rs21069481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	1904	1904	.	+	.	ID=625;Variant_seq=A;Dbxref=dbSNP_129:rs21069351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1908	1908	.	+	.	ID=626;Variant_seq=T;Dbxref=dbSNP_129:rs21069341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	1913	1913	.	+	.	ID=627;Variant_seq=A;Dbxref=dbSNP_129:rs21069321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046439.1	dbSNP	SNV	2237	2237	.	+	.	ID=628;Variant_seq=T;Dbxref=dbSNP_129:rs21068511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	2240	2240	.	+	.	ID=629;Variant_seq=A;Dbxref=dbSNP_129:rs21068501;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046439.1	dbSNP	SNV	2336	2336	.	+	.	ID=630;Variant_seq=T;Dbxref=dbSNP_129:rs19253347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046439.1	dbSNP	SNV	2450	2450	.	+	.	ID=631;Variant_seq=C;Dbxref=dbSNP_129:rs21068241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039700.1	dbSNP	SNV	1164	1164	.	+	.	ID=632;Variant_seq=G;Dbxref=dbSNP_129:rs21756455;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039700.1	dbSNP	SNV	1167	1167	.	+	.	ID=633;Variant_seq=T;Dbxref=dbSNP_129:rs21756473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039700.1	dbSNP	SNV	3891	3891	.	+	.	ID=634;Variant_seq=C;Dbxref=dbSNP_129:rs20195139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039700.1	dbSNP	SNV	3894	3894	.	+	.	ID=635;Variant_seq=T;Dbxref=dbSNP_129:rs20195129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400102.1	dbSNP	deletion	342	342	.	+	.	ID=636;Variant_seq=-;Dbxref=dbSNP_129:rs54087169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400102.1	dbSNP	SNV	343	343	.	+	.	ID=637;Variant_seq=G;Dbxref=dbSNP_129:rs53889700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400102.1	dbSNP	SNV	348	348	.	+	.	ID=638;Variant_seq=T;Dbxref=dbSNP_129:rs53398909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400102.1	dbSNP	SNV	367	367	.	+	.	ID=639;Variant_seq=A;Dbxref=dbSNP_129:rs53285596;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400102.1	dbSNP	SNV	406	406	.	+	.	ID=640;Variant_seq=C;Dbxref=dbSNP_129:rs53457410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400102.1	dbSNP	SNV	410	410	.	+	.	ID=641;Variant_seq=C;Dbxref=dbSNP_129:rs53309712;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400102.1	dbSNP	SNV	418	418	.	+	.	ID=642;Variant_seq=A;Dbxref=dbSNP_129:rs53542419;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400102.1	dbSNP	SNV	428	428	.	+	.	ID=643;Variant_seq=C;Dbxref=dbSNP_129:rs53260060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039348.1	dbSNP	SNV	1701	1701	.	+	.	ID=644;Variant_seq=A;Dbxref=dbSNP_129:rs20794164;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039348.1	dbSNP	SNV	5405	5405	.	+	.	ID=645;Variant_seq=A;Dbxref=dbSNP_129:rs19562461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	637	637	.	+	.	ID=646;Variant_seq=A;Dbxref=dbSNP_129:rs21654235;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	3310	3310	.	+	.	ID=647;Variant_seq=T;Dbxref=dbSNP_129:rs53617182;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398631.1	dbSNP	SNV	3335	3335	.	+	.	ID=648;Variant_seq=C;Dbxref=dbSNP_129:rs54176474;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398631.1	dbSNP	SNV	5860	5860	.	+	.	ID=649;Variant_seq=T;Dbxref=dbSNP_129:rs53617182;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398631.1	dbSNP	SNV	5885	5885	.	+	.	ID=650;Variant_seq=C;Dbxref=dbSNP_129:rs54176474;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398631.1	dbSNP	SNV	9512	9512	.	+	.	ID=651;Variant_seq=T;Dbxref=dbSNP_129:rs53645852;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398631.1	dbSNP	SNV	9518	9518	.	+	.	ID=652;Variant_seq=T;Dbxref=dbSNP_129:rs53910798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	10694	10694	.	+	.	ID=653;Variant_seq=G;Dbxref=dbSNP_129:rs54073660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398631.1	dbSNP	SNV	10760	10760	.	+	.	ID=654;Variant_seq=G;Dbxref=dbSNP_129:rs53869611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398631.1	dbSNP	SNV	10761	10761	.	+	.	ID=655;Variant_seq=A;Dbxref=dbSNP_129:rs53397172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	10764	10764	.	+	.	ID=656;Variant_seq=A;Dbxref=dbSNP_129:rs53436416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	10765	10765	.	+	.	ID=657;Variant_seq=A;Dbxref=dbSNP_129:rs54224795;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398631.1	dbSNP	SNV	10766	10766	.	+	.	ID=658;Variant_seq=T;Dbxref=dbSNP_129:rs53615380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	10767	10767	.	+	.	ID=659;Variant_seq=A;Dbxref=dbSNP_129:rs52899958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398631.1	dbSNP	SNV	10768	10768	.	+	.	ID=660;Variant_seq=T;Dbxref=dbSNP_129:rs54274692;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398631.1	dbSNP	SNV	10769	10769	.	+	.	ID=661;Variant_seq=A;Dbxref=dbSNP_129:rs53788307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050158.1	dbSNP	SNV	999	999	.	+	.	ID=662;Variant_seq=T;Dbxref=dbSNP_129:rs52973364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1000	1000	.	+	.	ID=663;Variant_seq=C;Dbxref=dbSNP_129:rs53180208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02050158.1	dbSNP	SNV	1135	1135	.	+	.	ID=664;Variant_seq=T;Dbxref=dbSNP_129:rs54333073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1151	1151	.	+	.	ID=665;Variant_seq=A,T,C;Dbxref=dbSNP_129:rs53232142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050158.1	dbSNP	SNV	1152	1152	.	+	.	ID=666;Variant_seq=T;Dbxref=dbSNP_129:rs53204457;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1155	1155	.	+	.	ID=667;Variant_seq=T;Dbxref=dbSNP_129:rs54305581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1158	1158	.	+	.	ID=668;Variant_seq=C;Dbxref=dbSNP_129:rs53645287;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050158.1	dbSNP	SNV	1159	1159	.	+	.	ID=669;Variant_seq=G;Dbxref=dbSNP_129:rs53359885;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1164	1164	.	+	.	ID=670;Variant_seq=A;Dbxref=dbSNP_129:rs54013983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050158.1	dbSNP	SNV	1168	1168	.	+	.	ID=671;Variant_seq=G;Dbxref=dbSNP_129:rs54012312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1171	1171	.	+	.	ID=672;Variant_seq=T;Dbxref=dbSNP_129:rs54175950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050158.1	dbSNP	SNV	1173	1173	.	+	.	ID=673;Variant_seq=A;Dbxref=dbSNP_129:rs53711458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050158.1	dbSNP	SNV	1174	1174	.	+	.	ID=674;Variant_seq=A;Dbxref=dbSNP_129:rs53989479;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049098.1	dbSNP	SNV	1159	1159	.	+	.	ID=675;Variant_seq=A;Dbxref=dbSNP_129:rs54107251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039089.1	dbSNP	SNV	142	142	.	+	.	ID=676;Variant_seq=C;Dbxref=dbSNP_129:rs19954407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039089.1	dbSNP	SNV	192	192	.	+	.	ID=677;Variant_seq=T;Dbxref=dbSNP_129:rs19954417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039089.1	dbSNP	SNV	781	781	.	+	.	ID=678;Variant_seq=T;Dbxref=dbSNP_129:rs19954497;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039089.1	dbSNP	SNV	794	794	.	+	.	ID=679;Variant_seq=A;Dbxref=dbSNP_129:rs19954507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039089.1	dbSNP	SNV	1948	1948	.	+	.	ID=680;Variant_seq=T;Dbxref=dbSNP_129:rs54087664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041093.1	dbSNP	SNV	1875	1875	.	+	.	ID=681;Variant_seq=C;Dbxref=dbSNP_129:rs21629730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041093.1	dbSNP	SNV	2222	2222	.	+	.	ID=682;Variant_seq=T;Dbxref=dbSNP_129:rs20009494;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041093.1	dbSNP	SNV	4329	4329	.	+	.	ID=683;Variant_seq=G;Dbxref=dbSNP_129:rs53667459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398731.1	dbSNP	SNV	1251	1251	.	+	.	ID=684;Variant_seq=A;Dbxref=dbSNP_129:rs19607115;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398731.1	dbSNP	SNV	5474	5474	.	+	.	ID=685;Variant_seq=G;Dbxref=dbSNP_129:rs21686657;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398731.1	dbSNP	SNV	8849	8849	.	+	.	ID=686;Variant_seq=A;Dbxref=dbSNP_129:rs53254261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398731.1	dbSNP	insertion	10415	10415	.	+	.	ID=687;Variant_seq=A;Dbxref=dbSNP_129:rs53192157;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02049212.1	dbSNP	SNV	1921	1921	.	+	.	ID=688;Variant_seq=T;Dbxref=dbSNP_129:rs20685168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	deletion	1703	1703	.	+	.	ID=689;Variant_seq=-;Dbxref=dbSNP_129:rs53531683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	1922	1922	.	+	.	ID=690;Variant_seq=G;Dbxref=dbSNP_129:rs21603255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399105.1	dbSNP	SNV	1934	1934	.	+	.	ID=691;Variant_seq=T;Dbxref=dbSNP_129:rs21603246;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399105.1	dbSNP	SNV	1939	1939	.	+	.	ID=692;Variant_seq=T;Dbxref=dbSNP_129:rs21603237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399105.1	dbSNP	SNV	1940	1940	.	+	.	ID=693;Variant_seq=A;Dbxref=dbSNP_129:rs21603228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399105.1	dbSNP	SNV	1960	1960	.	+	.	ID=694;Variant_seq=T;Dbxref=dbSNP_129:rs21603210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399105.1	dbSNP	SNV	1961	1961	.	+	.	ID=695;Variant_seq=G;Dbxref=dbSNP_129:rs21603201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	deletion	2006	2007	.	+	.	ID=696;Variant_seq=-;Dbxref=dbSNP_129:rs53644113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=CG
CH399105.1	dbSNP	SNV	2212	2212	.	+	.	ID=697;Variant_seq=G;Dbxref=dbSNP_129:rs18357450;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	2755	2755	.	+	.	ID=698;Variant_seq=T;Dbxref=dbSNP_129:rs53399938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399105.1	dbSNP	SNV	4860	4860	.	+	.	ID=699;Variant_seq=C;Dbxref=dbSNP_129:rs54049243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	4928	4928	.	+	.	ID=700;Variant_seq=C;Dbxref=dbSNP_129:rs53408765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	4934	4934	.	+	.	ID=701;Variant_seq=T;Dbxref=dbSNP_129:rs53554737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	5215	5215	.	+	.	ID=702;Variant_seq=G;Dbxref=dbSNP_129:rs53321039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399105.1	dbSNP	SNV	5339	5339	.	+	.	ID=703;Variant_seq=G;Dbxref=dbSNP_129:rs54122011;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398523.1	dbSNP	SNV	7325	7325	.	+	.	ID=704;Variant_seq=T;Dbxref=dbSNP_129:rs21155239;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398523.1	dbSNP	SNV	7665	7665	.	+	.	ID=705;Variant_seq=A;Dbxref=dbSNP_129:rs21155289;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398523.1	dbSNP	SNV	7780	7780	.	+	.	ID=706;Variant_seq=G;Dbxref=dbSNP_129:rs21155299;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398523.1	dbSNP	SNV	9245	9245	.	+	.	ID=707;Variant_seq=A;Dbxref=dbSNP_129:rs21155919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398523.1	dbSNP	SNV	9832	9832	.	+	.	ID=708;Variant_seq=T;Dbxref=dbSNP_129:rs21155969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398575.1	dbSNP	SNV	1800	1800	.	+	.	ID=709;Variant_seq=A;Dbxref=dbSNP_129:rs54372067;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398575.1	dbSNP	SNV	2714	2714	.	+	.	ID=710;Variant_seq=T;Dbxref=dbSNP_129:rs20294738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398575.1	dbSNP	SNV	3884	3884	.	+	.	ID=711;Variant_seq=A;Dbxref=dbSNP_129:rs19117716;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398575.1	dbSNP	SNV	4204	4204	.	+	.	ID=712;Variant_seq=G;Dbxref=dbSNP_129:rs19118156;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398575.1	dbSNP	SNV	9048	9048	.	+	.	ID=713;Variant_seq=G;Dbxref=dbSNP_129:rs21072698;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398575.1	dbSNP	SNV	9599	9599	.	+	.	ID=714;Variant_seq=T;Dbxref=dbSNP_129:rs21073098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398575.1	dbSNP	SNV	10287	10287	.	+	.	ID=715;Variant_seq=T;Dbxref=dbSNP_129:rs20294838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399617.1	dbSNP	SNV	1298	1298	.	+	.	ID=716;Variant_seq=A;Dbxref=dbSNP_129:rs53401747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399617.1	dbSNP	SNV	1368	1368	.	+	.	ID=717;Variant_seq=C;Dbxref=dbSNP_129:rs53901350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399617.1	dbSNP	SNV	1379	1379	.	+	.	ID=718;Variant_seq=A;Dbxref=dbSNP_129:rs53435964;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399617.1	dbSNP	SNV	1384	1384	.	+	.	ID=719;Variant_seq=T;Dbxref=dbSNP_129:rs53994255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399617.1	dbSNP	SNV	1388	1388	.	+	.	ID=720;Variant_seq=T;Dbxref=dbSNP_129:rs54247312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399617.1	dbSNP	SNV	1396	1396	.	+	.	ID=721;Variant_seq=A,T;Dbxref=dbSNP_129:rs53933232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399617.1	dbSNP	SNV	1405	1405	.	+	.	ID=722;Variant_seq=A;Dbxref=dbSNP_129:rs54047524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399617.1	dbSNP	SNV	1406	1406	.	+	.	ID=723;Variant_seq=G;Dbxref=dbSNP_129:rs54354483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399617.1	dbSNP	SNV	4480	4480	.	+	.	ID=724;Variant_seq=G;Dbxref=dbSNP_129:rs18862232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399617.1	dbSNP	SNV	4750	4750	.	+	.	ID=725;Variant_seq=A;Dbxref=dbSNP_129:rs18862222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040794.1	dbSNP	SNV	3369	3369	.	+	.	ID=726;Variant_seq=C;Dbxref=dbSNP_129:rs53531100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040794.1	dbSNP	SNV	4925	4925	.	+	.	ID=727;Variant_seq=T;Dbxref=dbSNP_129:rs20561556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398705.1	dbSNP	SNV	4822	4822	.	+	.	ID=728;Variant_seq=T;Dbxref=dbSNP_129:rs52981934;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	133	133	.	+	.	ID=729;Variant_seq=G;Dbxref=dbSNP_129:rs20759745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	253	253	.	+	.	ID=730;Variant_seq=C;Dbxref=dbSNP_129:rs20759765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	332	332	.	+	.	ID=731;Variant_seq=G;Dbxref=dbSNP_129:rs20759795;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	369	369	.	+	.	ID=732;Variant_seq=C;Dbxref=dbSNP_129:rs20759805;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	540	540	.	+	.	ID=733;Variant_seq=G;Dbxref=dbSNP_129:rs20759825;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	557	557	.	+	.	ID=734;Variant_seq=G;Dbxref=dbSNP_129:rs20759835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	830	830	.	+	.	ID=735;Variant_seq=C;Dbxref=dbSNP_129:rs53977853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	886	886	.	+	.	ID=736;Variant_seq=T;Dbxref=dbSNP_129:rs20162302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	2678	2678	.	+	.	ID=737;Variant_seq=A;Dbxref=dbSNP_129:rs20759915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399994.1	dbSNP	SNV	2690	2690	.	+	.	ID=738;Variant_seq=A;Dbxref=dbSNP_129:rs20759925;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	2770	2770	.	+	.	ID=739;Variant_seq=A;Dbxref=dbSNP_129:rs20759935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399994.1	dbSNP	SNV	2876	2876	.	+	.	ID=740;Variant_seq=T;Dbxref=dbSNP_129:rs20459067;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	2955	2955	.	+	.	ID=741;Variant_seq=T;Dbxref=dbSNP_129:rs20759975;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3040	3040	.	+	.	ID=742;Variant_seq=A;Dbxref=dbSNP_129:rs20759995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399994.1	dbSNP	SNV	3067	3067	.	+	.	ID=743;Variant_seq=T;Dbxref=dbSNP_129:rs20760005;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	3122	3122	.	+	.	ID=744;Variant_seq=C;Dbxref=dbSNP_129:rs20760025;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	3171	3171	.	+	.	ID=745;Variant_seq=C;Dbxref=dbSNP_129:rs20760035;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	3192	3192	.	+	.	ID=746;Variant_seq=G;Dbxref=dbSNP_129:rs20760045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3229	3229	.	+	.	ID=747;Variant_seq=G;Dbxref=dbSNP_129:rs20760055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	3340	3340	.	+	.	ID=748;Variant_seq=T;Dbxref=dbSNP_129:rs20760065;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	3348	3348	.	+	.	ID=749;Variant_seq=G;Dbxref=dbSNP_129:rs20760075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3404	3404	.	+	.	ID=750;Variant_seq=A;Dbxref=dbSNP_129:rs20760085;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399994.1	dbSNP	SNV	3420	3420	.	+	.	ID=751;Variant_seq=G;Dbxref=dbSNP_129:rs20760095;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3586	3586	.	+	.	ID=752;Variant_seq=G;Dbxref=dbSNP_129:rs20760145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3615	3615	.	+	.	ID=753;Variant_seq=A;Dbxref=dbSNP_129:rs20760155;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399994.1	dbSNP	SNV	3626	3626	.	+	.	ID=754;Variant_seq=C;Dbxref=dbSNP_129:rs20760165;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399994.1	dbSNP	SNV	3670	3670	.	+	.	ID=755;Variant_seq=G;Dbxref=dbSNP_129:rs20760175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3745	3745	.	+	.	ID=756;Variant_seq=G;Dbxref=dbSNP_129:rs20760185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399994.1	dbSNP	SNV	3827	3827	.	+	.	ID=757;Variant_seq=T;Dbxref=dbSNP_129:rs20760195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	3839	3839	.	+	.	ID=758;Variant_seq=T;Dbxref=dbSNP_129:rs20760205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399994.1	dbSNP	SNV	3892	3892	.	+	.	ID=759;Variant_seq=A;Dbxref=dbSNP_129:rs20760215;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048220.1	dbSNP	SNV	1506	1506	.	+	.	ID=760;Variant_seq=G;Dbxref=dbSNP_129:rs54272416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048220.1	dbSNP	SNV	1506	1506	.	+	.	ID=761;Variant_seq=G;Dbxref=dbSNP_129:rs54199985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048220.1	dbSNP	SNV	1518	1518	.	+	.	ID=762;Variant_seq=T;Dbxref=dbSNP_129:rs53570555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048220.1	dbSNP	SNV	1954	1954	.	+	.	ID=763;Variant_seq=A,T;Dbxref=dbSNP_129:rs54114954;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400369.1	dbSNP	SNV	202	202	.	+	.	ID=764;Variant_seq=C;Dbxref=dbSNP_129:rs21019242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	216	216	.	+	.	ID=765;Variant_seq=C;Dbxref=dbSNP_129:rs21019262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	227	227	.	+	.	ID=766;Variant_seq=C;Dbxref=dbSNP_129:rs21019282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	256	256	.	+	.	ID=767;Variant_seq=A;Dbxref=dbSNP_129:rs21019292;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400369.1	dbSNP	SNV	311	311	.	+	.	ID=768;Variant_seq=G;Dbxref=dbSNP_129:rs21019302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400369.1	dbSNP	SNV	456	456	.	+	.	ID=769;Variant_seq=T;Dbxref=dbSNP_129:rs21019312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	601	601	.	+	.	ID=770;Variant_seq=C;Dbxref=dbSNP_129:rs21019322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	819	819	.	+	.	ID=771;Variant_seq=T;Dbxref=dbSNP_129:rs21019342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	1033	1033	.	+	.	ID=772;Variant_seq=T;Dbxref=dbSNP_129:rs21019352;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	1164	1164	.	+	.	ID=773;Variant_seq=C;Dbxref=dbSNP_129:rs21019372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400369.1	dbSNP	SNV	1346	1346	.	+	.	ID=774;Variant_seq=T;Dbxref=dbSNP_129:rs21019382;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	1401	1401	.	+	.	ID=775;Variant_seq=A;Dbxref=dbSNP_129:rs21019392;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400369.1	dbSNP	SNV	1737	1737	.	+	.	ID=776;Variant_seq=T;Dbxref=dbSNP_129:rs21019522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	1792	1792	.	+	.	ID=777;Variant_seq=A;Dbxref=dbSNP_129:rs21019532;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400369.1	dbSNP	SNV	1804	1804	.	+	.	ID=778;Variant_seq=A;Dbxref=dbSNP_129:rs21019542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400369.1	dbSNP	SNV	1955	1955	.	+	.	ID=779;Variant_seq=A;Dbxref=dbSNP_129:rs21019562;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	2195	2195	.	+	.	ID=780;Variant_seq=T;Dbxref=dbSNP_129:rs21705346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400369.1	dbSNP	SNV	2196	2196	.	+	.	ID=781;Variant_seq=T;Dbxref=dbSNP_129:rs18507499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	2627	2627	.	+	.	ID=782;Variant_seq=T;Dbxref=dbSNP_129:rs21019642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400369.1	dbSNP	SNV	2921	2921	.	+	.	ID=783;Variant_seq=A;Dbxref=dbSNP_129:rs21019702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	3045	3045	.	+	.	ID=784;Variant_seq=C;Dbxref=dbSNP_129:rs21019722;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400369.1	dbSNP	SNV	3087	3087	.	+	.	ID=785;Variant_seq=T;Dbxref=dbSNP_129:rs21019732;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048385.1	dbSNP	SNV	463	463	.	+	.	ID=786;Variant_seq=T;Dbxref=dbSNP_129:rs53975446;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048385.1	dbSNP	SNV	596	596	.	+	.	ID=787;Variant_seq=C;Dbxref=dbSNP_129:rs53599436;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048385.1	dbSNP	SNV	1388	1388	.	+	.	ID=788;Variant_seq=A;Dbxref=dbSNP_129:rs21696646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398683.1	dbSNP	SNV	1125	1125	.	+	.	ID=789;Variant_seq=C;Dbxref=dbSNP_129:rs21016237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398683.1	dbSNP	SNV	2454	2454	.	+	.	ID=790;Variant_seq=T;Dbxref=dbSNP_129:rs18589901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398683.1	dbSNP	SNV	2483	2483	.	+	.	ID=791;Variant_seq=T;Dbxref=dbSNP_129:rs18589892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398683.1	dbSNP	SNV	2497	2497	.	+	.	ID=792;Variant_seq=T;Dbxref=dbSNP_129:rs18044412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398683.1	dbSNP	SNV	5896	5896	.	+	.	ID=793;Variant_seq=G;Dbxref=dbSNP_129:rs19491342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398683.1	dbSNP	SNV	5897	5897	.	+	.	ID=794;Variant_seq=A;Dbxref=dbSNP_129:rs19491332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398683.1	dbSNP	SNV	5900	5900	.	+	.	ID=795;Variant_seq=T;Dbxref=dbSNP_129:rs19491322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398683.1	dbSNP	SNV	6190	6190	.	+	.	ID=796;Variant_seq=C;Dbxref=dbSNP_129:rs18934506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398683.1	dbSNP	SNV	6197	6197	.	+	.	ID=797;Variant_seq=C;Dbxref=dbSNP_129:rs18934496;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398683.1	dbSNP	SNV	9900	9900	.	+	.	ID=798;Variant_seq=A;Dbxref=dbSNP_129:rs53508441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044538.1	dbSNP	SNV	746	746	.	+	.	ID=799;Variant_seq=T;Dbxref=dbSNP_129:rs53267767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044538.1	dbSNP	SNV	918	918	.	+	.	ID=800;Variant_seq=C;Dbxref=dbSNP_129:rs53035743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400626.1	dbSNP	SNV	501	501	.	+	.	ID=801;Variant_seq=A;Dbxref=dbSNP_129:rs52979396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400626.1	dbSNP	SNV	965	965	.	+	.	ID=802;Variant_seq=A;Dbxref=dbSNP_129:rs52979396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400626.1	dbSNP	SNV	1337	1337	.	+	.	ID=803;Variant_seq=A;Dbxref=dbSNP_129:rs18187928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399584.1	dbSNP	SNV	1139	1139	.	+	.	ID=804;Variant_seq=C;Dbxref=dbSNP_129:rs53939148;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399584.1	dbSNP	SNV	1436	1436	.	+	.	ID=805;Variant_seq=T;Dbxref=dbSNP_129:rs54384549;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	1478	1478	.	+	.	ID=806;Variant_seq=A;Dbxref=dbSNP_129:rs52940180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399584.1	dbSNP	SNV	1480	1480	.	+	.	ID=807;Variant_seq=A;Dbxref=dbSNP_129:rs53643222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399584.1	dbSNP	deletion	1521	1521	.	+	.	ID=808;Variant_seq=-;Dbxref=dbSNP_129:rs53212604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	1576	1576	.	+	.	ID=809;Variant_seq=T;Dbxref=dbSNP_129:rs54300740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	1614	1614	.	+	.	ID=810;Variant_seq=T;Dbxref=dbSNP_129:rs53359821;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	1673	1673	.	+	.	ID=811;Variant_seq=C;Dbxref=dbSNP_129:rs18198848;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399584.1	dbSNP	SNV	1706	1706	.	+	.	ID=812;Variant_seq=A;Dbxref=dbSNP_129:rs18198857;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399584.1	dbSNP	SNV	1760	1760	.	+	.	ID=813;Variant_seq=C;Dbxref=dbSNP_129:rs18198911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399584.1	dbSNP	SNV	1945	1945	.	+	.	ID=814;Variant_seq=G;Dbxref=dbSNP_129:rs18199136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399584.1	dbSNP	SNV	1963	1963	.	+	.	ID=815;Variant_seq=T;Dbxref=dbSNP_129:rs18199153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	2472	2472	.	+	.	ID=816;Variant_seq=T;Dbxref=dbSNP_129:rs21566735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399584.1	dbSNP	SNV	2474	2474	.	+	.	ID=817;Variant_seq=C;Dbxref=dbSNP_129:rs21566725;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399584.1	dbSNP	SNV	2476	2476	.	+	.	ID=818;Variant_seq=T;Dbxref=dbSNP_129:rs21566715;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399584.1	dbSNP	SNV	2499	2499	.	+	.	ID=819;Variant_seq=T;Dbxref=dbSNP_129:rs21031517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399584.1	dbSNP	SNV	2594	2594	.	+	.	ID=820;Variant_seq=G;Dbxref=dbSNP_129:rs18199414;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399584.1	dbSNP	SNV	4844	4844	.	+	.	ID=821;Variant_seq=G;Dbxref=dbSNP_129:rs21039523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400204.1	dbSNP	SNV	1778	1778	.	+	.	ID=822;Variant_seq=T;Dbxref=dbSNP_129:rs20254875;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400204.1	dbSNP	SNV	1970	1970	.	+	.	ID=823;Variant_seq=C;Dbxref=dbSNP_129:rs20252985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400204.1	dbSNP	SNV	2913	2913	.	+	.	ID=824;Variant_seq=A;Dbxref=dbSNP_129:rs20255065;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400204.1	dbSNP	SNV	2914	2914	.	+	.	ID=825;Variant_seq=T;Dbxref=dbSNP_129:rs20255075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400204.1	dbSNP	SNV	2935	2935	.	+	.	ID=826;Variant_seq=A;Dbxref=dbSNP_129:rs20255085;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400204.1	dbSNP	SNV	2936	2936	.	+	.	ID=827;Variant_seq=C;Dbxref=dbSNP_129:rs20255095;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400204.1	dbSNP	insertion	3164	3164	.	+	.	ID=828;Variant_seq=GAT;Dbxref=dbSNP_129:rs53306982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH399792.1	dbSNP	SNV	3005	3005	.	+	.	ID=829;Variant_seq=T;Dbxref=dbSNP_129:rs19891557;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041611.1	dbSNP	SNV	1529	1529	.	+	.	ID=830;Variant_seq=A;Dbxref=dbSNP_129:rs54249481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041611.1	dbSNP	SNV	1542	1542	.	+	.	ID=831;Variant_seq=C;Dbxref=dbSNP_129:rs53192790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041611.1	dbSNP	SNV	1546	1546	.	+	.	ID=832;Variant_seq=A;Dbxref=dbSNP_129:rs52973649;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041611.1	dbSNP	SNV	1574	1574	.	+	.	ID=833;Variant_seq=G;Dbxref=dbSNP_129:rs53921427;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041611.1	dbSNP	SNV	1580	1580	.	+	.	ID=834;Variant_seq=A;Dbxref=dbSNP_129:rs53944195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041611.1	dbSNP	SNV	1590	1590	.	+	.	ID=835;Variant_seq=A;Dbxref=dbSNP_129:rs54107785;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041611.1	dbSNP	SNV	1593	1593	.	+	.	ID=836;Variant_seq=T;Dbxref=dbSNP_129:rs52996765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041611.1	dbSNP	SNV	2239	2239	.	+	.	ID=837;Variant_seq=C;Dbxref=dbSNP_129:rs52972024;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041611.1	dbSNP	SNV	2239	2239	.	+	.	ID=838;Variant_seq=T,G;Dbxref=dbSNP_129:rs52854128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399549.1	dbSNP	SNV	2589	2589	.	+	.	ID=839;Variant_seq=T;Dbxref=dbSNP_129:rs20045103;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399549.1	dbSNP	SNV	2666	2666	.	+	.	ID=840;Variant_seq=A;Dbxref=dbSNP_129:rs52920757;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399549.1	dbSNP	SNV	2680	2680	.	+	.	ID=841;Variant_seq=T;Dbxref=dbSNP_129:rs53903453;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399549.1	dbSNP	SNV	2690	2690	.	+	.	ID=842;Variant_seq=A;Dbxref=dbSNP_129:rs53265102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399549.1	dbSNP	SNV	2749	2749	.	+	.	ID=843;Variant_seq=T;Dbxref=dbSNP_129:rs54150471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042737.1	dbSNP	SNV	3405	3405	.	+	.	ID=844;Variant_seq=C;Dbxref=dbSNP_129:rs21435875;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049821.1	dbSNP	SNV	274	274	.	+	.	ID=845;Variant_seq=A;Dbxref=dbSNP_129:rs52991198;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049821.1	dbSNP	SNV	474	474	.	+	.	ID=846;Variant_seq=T;Dbxref=dbSNP_129:rs19112668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049821.1	dbSNP	SNV	544	544	.	+	.	ID=847;Variant_seq=T;Dbxref=dbSNP_129:rs19112658;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049821.1	dbSNP	SNV	687	687	.	+	.	ID=848;Variant_seq=T;Dbxref=dbSNP_129:rs53253492;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049821.1	dbSNP	SNV	1325	1325	.	+	.	ID=849;Variant_seq=A;Dbxref=dbSNP_129:rs53267786;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049821.1	dbSNP	SNV	1329	1329	.	+	.	ID=850;Variant_seq=C;Dbxref=dbSNP_129:rs52902544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043507.1	dbSNP	SNV	121	121	.	+	.	ID=851;Variant_seq=T;Dbxref=dbSNP_129:rs53463733;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043507.1	dbSNP	SNV	784	784	.	+	.	ID=852;Variant_seq=T;Dbxref=dbSNP_129:rs54382199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043507.1	dbSNP	SNV	784	784	.	+	.	ID=853;Variant_seq=A;Dbxref=dbSNP_129:rs53400231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043507.1	dbSNP	SNV	869	869	.	+	.	ID=854;Variant_seq=T;Dbxref=dbSNP_129:rs53628036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043507.1	dbSNP	SNV	1101	1101	.	+	.	ID=855;Variant_seq=T;Dbxref=dbSNP_129:rs53650348;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043507.1	dbSNP	SNV	2098	2098	.	+	.	ID=856;Variant_seq=G;Dbxref=dbSNP_129:rs52895744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043507.1	dbSNP	SNV	2152	2152	.	+	.	ID=857;Variant_seq=A;Dbxref=dbSNP_129:rs53848188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043507.1	dbSNP	SNV	2153	2153	.	+	.	ID=858;Variant_seq=C;Dbxref=dbSNP_129:rs53009242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043507.1	dbSNP	SNV	2223	2223	.	+	.	ID=859;Variant_seq=A;Dbxref=dbSNP_129:rs52981824;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399528.1	dbSNP	SNV	2425	2425	.	+	.	ID=860;Variant_seq=A;Dbxref=dbSNP_129:rs20350081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399528.1	dbSNP	SNV	3016	3016	.	+	.	ID=861;Variant_seq=T;Dbxref=dbSNP_129:rs21756868;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039905.1	dbSNP	SNV	2925	2925	.	+	.	ID=862;Variant_seq=A;Dbxref=dbSNP_129:rs20901895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039905.1	dbSNP	SNV	3598	3598	.	+	.	ID=863;Variant_seq=T;Dbxref=dbSNP_129:rs20902225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399304.1	dbSNP	SNV	447	447	.	+	.	ID=864;Variant_seq=G;Dbxref=dbSNP_129:rs52856888;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399304.1	dbSNP	SNV	449	449	.	+	.	ID=865;Variant_seq=G;Dbxref=dbSNP_129:rs53625575;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399304.1	dbSNP	SNV	450	450	.	+	.	ID=866;Variant_seq=G;Dbxref=dbSNP_129:rs54199102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399304.1	dbSNP	SNV	451	451	.	+	.	ID=867;Variant_seq=G;Dbxref=dbSNP_129:rs53208057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399304.1	dbSNP	deletion	454	455	.	+	.	ID=868;Variant_seq=-;Dbxref=dbSNP_129:rs54140102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=GC
CH399304.1	dbSNP	SNV	455	455	.	+	.	ID=869;Variant_seq=A;Dbxref=dbSNP_129:rs52866271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399304.1	dbSNP	SNV	473	473	.	+	.	ID=870;Variant_seq=T;Dbxref=dbSNP_129:rs53661898;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399304.1	dbSNP	SNV	478	478	.	+	.	ID=871;Variant_seq=T;Dbxref=dbSNP_129:rs53021588;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399304.1	dbSNP	SNV	482	482	.	+	.	ID=872;Variant_seq=A;Dbxref=dbSNP_129:rs53477682;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399304.1	dbSNP	SNV	2011	2011	.	+	.	ID=873;Variant_seq=A;Dbxref=dbSNP_129:rs53979652;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399304.1	dbSNP	SNV	5810	5810	.	+	.	ID=874;Variant_seq=C;Dbxref=dbSNP_129:rs20797905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399304.1	dbSNP	SNV	5811	5811	.	+	.	ID=875;Variant_seq=C;Dbxref=dbSNP_129:rs20797895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399304.1	dbSNP	SNV	5813	5813	.	+	.	ID=876;Variant_seq=A,T,C;Dbxref=dbSNP_129:rs17889944;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398882.1	dbSNP	SNV	829	829	.	+	.	ID=877;Variant_seq=T;Dbxref=dbSNP_129:rs20426052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398882.1	dbSNP	SNV	6933	6933	.	+	.	ID=878;Variant_seq=A;Dbxref=dbSNP_129:rs20643240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398882.1	dbSNP	SNV	7806	7806	.	+	.	ID=879;Variant_seq=T;Dbxref=dbSNP_129:rs53078083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398882.1	dbSNP	SNV	7843	7843	.	+	.	ID=880;Variant_seq=A;Dbxref=dbSNP_129:rs54238896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398882.1	dbSNP	SNV	7966	7966	.	+	.	ID=881;Variant_seq=A;Dbxref=dbSNP_129:rs20819651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398882.1	dbSNP	SNV	8137	8137	.	+	.	ID=882;Variant_seq=T;Dbxref=dbSNP_129:rs18764508;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399481.1	dbSNP	SNV	327	327	.	+	.	ID=883;Variant_seq=A;Dbxref=dbSNP_129:rs21504793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399481.1	dbSNP	SNV	412	412	.	+	.	ID=884;Variant_seq=T;Dbxref=dbSNP_129:rs21504803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399481.1	dbSNP	SNV	1169	1169	.	+	.	ID=885;Variant_seq=T;Dbxref=dbSNP_129:rs21504843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399481.1	dbSNP	SNV	2353	2353	.	+	.	ID=886;Variant_seq=A;Dbxref=dbSNP_129:rs20404403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048871.1	dbSNP	SNV	885	885	.	+	.	ID=887;Variant_seq=T;Dbxref=dbSNP_129:rs20236563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048871.1	dbSNP	SNV	910	910	.	+	.	ID=888;Variant_seq=A;Dbxref=dbSNP_129:rs20173812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048871.1	dbSNP	SNV	927	927	.	+	.	ID=889;Variant_seq=G;Dbxref=dbSNP_129:rs20236573;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048871.1	dbSNP	SNV	1337	1337	.	+	.	ID=890;Variant_seq=T;Dbxref=dbSNP_129:rs18810918;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048401.1	dbSNP	SNV	530	530	.	+	.	ID=891;Variant_seq=G;Dbxref=dbSNP_129:rs19071700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039610.1	dbSNP	SNV	278	278	.	+	.	ID=892;Variant_seq=C;Dbxref=dbSNP_129:rs21077459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039610.1	dbSNP	SNV	278	278	.	+	.	ID=893;Variant_seq=C;Dbxref=dbSNP_129:rs20433516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039610.1	dbSNP	SNV	453	453	.	+	.	ID=894;Variant_seq=T;Dbxref=dbSNP_129:rs20577511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039610.1	dbSNP	SNV	537	537	.	+	.	ID=895;Variant_seq=T;Dbxref=dbSNP_129:rs20577621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039610.1	dbSNP	SNV	1853	1853	.	+	.	ID=896;Variant_seq=C;Dbxref=dbSNP_129:rs54289651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399267.1	dbSNP	SNV	283	283	.	+	.	ID=897;Variant_seq=T;Dbxref=dbSNP_129:rs53097601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399267.1	dbSNP	SNV	586	586	.	+	.	ID=898;Variant_seq=G;Dbxref=dbSNP_129:rs21130629;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399267.1	dbSNP	SNV	708	708	.	+	.	ID=899;Variant_seq=T;Dbxref=dbSNP_129:rs18810685;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399267.1	dbSNP	SNV	3289	3289	.	+	.	ID=900;Variant_seq=A;Dbxref=dbSNP_129:rs53935390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399267.1	dbSNP	SNV	3292	3292	.	+	.	ID=901;Variant_seq=G;Dbxref=dbSNP_129:rs21168218;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399267.1	dbSNP	SNV	3300	3300	.	+	.	ID=902;Variant_seq=A;Dbxref=dbSNP_129:rs21168188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399267.1	dbSNP	SNV	3337	3337	.	+	.	ID=903;Variant_seq=G;Dbxref=dbSNP_129:rs53298316;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398897.1	dbSNP	SNV	764	764	.	+	.	ID=904;Variant_seq=T;Dbxref=dbSNP_129:rs21544208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398897.1	dbSNP	SNV	1527	1527	.	+	.	ID=905;Variant_seq=G;Dbxref=dbSNP_129:rs19560192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398897.1	dbSNP	SNV	1979	1979	.	+	.	ID=906;Variant_seq=A;Dbxref=dbSNP_129:rs19297163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398897.1	dbSNP	SNV	4286	4286	.	+	.	ID=907;Variant_seq=T;Dbxref=dbSNP_129:rs52997832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398897.1	dbSNP	SNV	7559	7559	.	+	.	ID=908;Variant_seq=G;Dbxref=dbSNP_129:rs54327080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040746.1	dbSNP	SNV	244	244	.	+	.	ID=909;Variant_seq=G;Dbxref=dbSNP_129:rs54379303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040746.1	dbSNP	SNV	4100	4100	.	+	.	ID=910;Variant_seq=C;Dbxref=dbSNP_129:rs20343791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	669	669	.	+	.	ID=911;Variant_seq=A;Dbxref=dbSNP_129:rs53506433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	1733	1733	.	+	.	ID=912;Variant_seq=A;Dbxref=dbSNP_129:rs54290499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	1734	1734	.	+	.	ID=913;Variant_seq=A;Dbxref=dbSNP_129:rs53959394;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	1737	1737	.	+	.	ID=914;Variant_seq=T;Dbxref=dbSNP_129:rs53138298;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2145	2145	.	+	.	ID=915;Variant_seq=G;Dbxref=dbSNP_129:rs53448351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2147	2147	.	+	.	ID=916;Variant_seq=T;Dbxref=dbSNP_129:rs53037810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2149	2149	.	+	.	ID=917;Variant_seq=C;Dbxref=dbSNP_129:rs54044879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2154	2154	.	+	.	ID=918;Variant_seq=G;Dbxref=dbSNP_129:rs54131873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2155	2155	.	+	.	ID=919;Variant_seq=C;Dbxref=dbSNP_129:rs53737053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	2160	2160	.	+	.	ID=920;Variant_seq=T;Dbxref=dbSNP_129:rs53605018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2163	2163	.	+	.	ID=921;Variant_seq=G;Dbxref=dbSNP_129:rs53208022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2164	2164	.	+	.	ID=922;Variant_seq=G;Dbxref=dbSNP_129:rs54110039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2167	2167	.	+	.	ID=923;Variant_seq=A,T;Dbxref=dbSNP_129:rs53164093;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2173	2173	.	+	.	ID=924;Variant_seq=G;Dbxref=dbSNP_129:rs53036221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2175	2175	.	+	.	ID=925;Variant_seq=C;Dbxref=dbSNP_129:rs53183927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	2209	2209	.	+	.	ID=926;Variant_seq=C;Dbxref=dbSNP_129:rs53503981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	2210	2210	.	+	.	ID=927;Variant_seq=A;Dbxref=dbSNP_129:rs53329637;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2214	2214	.	+	.	ID=928;Variant_seq=G;Dbxref=dbSNP_129:rs52859133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	deletion	2214	2215	.	+	.	ID=929;Variant_seq=-;Dbxref=dbSNP_129:rs52991914;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TC
CH399619.1	dbSNP	SNV	2219	2219	.	+	.	ID=930;Variant_seq=G;Dbxref=dbSNP_129:rs54369228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2222	2222	.	+	.	ID=931;Variant_seq=G;Dbxref=dbSNP_129:rs53562885;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	deletion	2224	2224	.	+	.	ID=932;Variant_seq=-;Dbxref=dbSNP_129:rs53577435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2226	2226	.	+	.	ID=933;Variant_seq=A;Dbxref=dbSNP_129:rs53736659;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	deletion	2229	2229	.	+	.	ID=934;Variant_seq=-;Dbxref=dbSNP_129:rs52992474;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2273	2273	.	+	.	ID=935;Variant_seq=T;Dbxref=dbSNP_129:rs53887793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2278	2278	.	+	.	ID=936;Variant_seq=T;Dbxref=dbSNP_129:rs52971609;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2280	2280	.	+	.	ID=937;Variant_seq=T;Dbxref=dbSNP_129:rs54389982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2281	2281	.	+	.	ID=938;Variant_seq=G;Dbxref=dbSNP_129:rs54161747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2282	2282	.	+	.	ID=939;Variant_seq=T;Dbxref=dbSNP_129:rs53946240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399619.1	dbSNP	SNV	2288	2288	.	+	.	ID=940;Variant_seq=A;Dbxref=dbSNP_129:rs54308868;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	2289	2289	.	+	.	ID=941;Variant_seq=A;Dbxref=dbSNP_129:rs54217068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2296	2296	.	+	.	ID=942;Variant_seq=T;Dbxref=dbSNP_129:rs53474714;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2302	2302	.	+	.	ID=943;Variant_seq=A;Dbxref=dbSNP_129:rs53398611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399619.1	dbSNP	SNV	2304	2304	.	+	.	ID=944;Variant_seq=G;Dbxref=dbSNP_129:rs54383325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2305	2305	.	+	.	ID=945;Variant_seq=C;Dbxref=dbSNP_129:rs54290168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	insertion	2305	2305	.	+	.	ID=946;Variant_seq=A;Dbxref=dbSNP_129:rs53315674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH399619.1	dbSNP	SNV	2306	2306	.	+	.	ID=947;Variant_seq=G;Dbxref=dbSNP_129:rs53307614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2307	2307	.	+	.	ID=948;Variant_seq=G;Dbxref=dbSNP_129:rs53620722;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	SNV	2308	2308	.	+	.	ID=949;Variant_seq=G;Dbxref=dbSNP_129:rs53399433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399619.1	dbSNP	insertion	2309	2309	.	+	.	ID=950;Variant_seq=AA;Dbxref=dbSNP_129:rs53544125;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH399619.1	dbSNP	SNV	2310	2310	.	+	.	ID=951;Variant_seq=A;Dbxref=dbSNP_129:rs54278978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2313	2313	.	+	.	ID=952;Variant_seq=A;Dbxref=dbSNP_129:rs54407666;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399619.1	dbSNP	SNV	2414	2414	.	+	.	ID=953;Variant_seq=T;Dbxref=dbSNP_129:rs20442487;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045345.1	dbSNP	SNV	87	87	.	+	.	ID=954;Variant_seq=A;Dbxref=dbSNP_129:rs20771661;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045345.1	dbSNP	SNV	404	404	.	+	.	ID=955;Variant_seq=T;Dbxref=dbSNP_129:rs20771831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400292.1	dbSNP	SNV	244	244	.	+	.	ID=956;Variant_seq=G;Dbxref=dbSNP_129:rs52973808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400292.1	dbSNP	SNV	1847	1847	.	+	.	ID=957;Variant_seq=C;Dbxref=dbSNP_129:rs20741100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399712.1	dbSNP	SNV	1732	1732	.	+	.	ID=958;Variant_seq=A;Dbxref=dbSNP_129:rs53940511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036780.1	dbSNP	SNV	7401	7401	.	+	.	ID=959;Variant_seq=A;Dbxref=dbSNP_129:rs20764575;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036780.1	dbSNP	SNV	7680	7680	.	+	.	ID=960;Variant_seq=T;Dbxref=dbSNP_129:rs20764675;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036780.1	dbSNP	SNV	7832	7832	.	+	.	ID=961;Variant_seq=C;Dbxref=dbSNP_129:rs20764755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036780.1	dbSNP	SNV	7836	7836	.	+	.	ID=962;Variant_seq=C;Dbxref=dbSNP_129:rs20764765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036780.1	dbSNP	SNV	7990	7990	.	+	.	ID=963;Variant_seq=A;Dbxref=dbSNP_129:rs20764815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036780.1	dbSNP	SNV	9794	9794	.	+	.	ID=964;Variant_seq=A;Dbxref=dbSNP_129:rs54037556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036780.1	dbSNP	SNV	10382	10382	.	+	.	ID=965;Variant_seq=A;Dbxref=dbSNP_129:rs21728327;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047043.1	dbSNP	SNV	1921	1921	.	+	.	ID=966;Variant_seq=A;Dbxref=dbSNP_129:rs20656280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047043.1	dbSNP	SNV	1929	1929	.	+	.	ID=967;Variant_seq=G;Dbxref=dbSNP_129:rs20656260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048652.1	dbSNP	SNV	1479	1479	.	+	.	ID=968;Variant_seq=G;Dbxref=dbSNP_129:rs19103904;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041051.1	dbSNP	SNV	707	707	.	+	.	ID=969;Variant_seq=A;Dbxref=dbSNP_129:rs18658716;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041051.1	dbSNP	SNV	713	713	.	+	.	ID=970;Variant_seq=A;Dbxref=dbSNP_129:rs18658725;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041051.1	dbSNP	SNV	719	719	.	+	.	ID=971;Variant_seq=A;Dbxref=dbSNP_129:rs18658752;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041051.1	dbSNP	SNV	724	724	.	+	.	ID=972;Variant_seq=G;Dbxref=dbSNP_129:rs18658770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041051.1	dbSNP	SNV	737	737	.	+	.	ID=973;Variant_seq=T,G;Dbxref=dbSNP_129:rs17901744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041051.1	dbSNP	SNV	1389	1389	.	+	.	ID=974;Variant_seq=C;Dbxref=dbSNP_129:rs53033554;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041051.1	dbSNP	insertion	1389	1389	.	+	.	ID=975;Variant_seq=G;Dbxref=dbSNP_129:rs53312626;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02041051.1	dbSNP	SNV	3409	3409	.	+	.	ID=976;Variant_seq=C;Dbxref=dbSNP_129:rs21252459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041051.1	dbSNP	SNV	3532	3532	.	+	.	ID=977;Variant_seq=C;Dbxref=dbSNP_129:rs53306012;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	1142	1142	.	+	.	ID=978;Variant_seq=A;Dbxref=dbSNP_129:rs21079041;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	1143	1143	.	+	.	ID=979;Variant_seq=A;Dbxref=dbSNP_129:rs21079031;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	1144	1144	.	+	.	ID=980;Variant_seq=A;Dbxref=dbSNP_129:rs21079021;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	1150	1150	.	+	.	ID=981;Variant_seq=A;Dbxref=dbSNP_129:rs21079001;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	3767	3767	.	+	.	ID=982;Variant_seq=A;Dbxref=dbSNP_129:rs21050706;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	4001	4001	.	+	.	ID=983;Variant_seq=G;Dbxref=dbSNP_129:rs21050523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398416.1	dbSNP	deletion	7497	7497	.	+	.	ID=984;Variant_seq=-;Dbxref=dbSNP_129:rs53066582;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	7530	7530	.	+	.	ID=985;Variant_seq=G;Dbxref=dbSNP_129:rs53407024;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	7601	7601	.	+	.	ID=986;Variant_seq=G;Dbxref=dbSNP_129:rs54151829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	7619	7619	.	+	.	ID=987;Variant_seq=A;Dbxref=dbSNP_129:rs52939421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	8078	8078	.	+	.	ID=988;Variant_seq=G;Dbxref=dbSNP_129:rs54198765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398416.1	dbSNP	SNV	12640	12640	.	+	.	ID=989;Variant_seq=G;Dbxref=dbSNP_129:rs53525680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398416.1	dbSNP	SNV	12681	12681	.	+	.	ID=990;Variant_seq=A;Dbxref=dbSNP_129:rs53871006;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	15496	15496	.	+	.	ID=991;Variant_seq=T;Dbxref=dbSNP_129:rs54108816;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	15516	15516	.	+	.	ID=992;Variant_seq=T;Dbxref=dbSNP_129:rs53390303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	15528	15528	.	+	.	ID=993;Variant_seq=A;Dbxref=dbSNP_129:rs53582878;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	15529	15529	.	+	.	ID=994;Variant_seq=C;Dbxref=dbSNP_129:rs53530640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	15532	15532	.	+	.	ID=995;Variant_seq=C;Dbxref=dbSNP_129:rs54161793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	15548	15548	.	+	.	ID=996;Variant_seq=T;Dbxref=dbSNP_129:rs53494602;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	16521	16521	.	+	.	ID=997;Variant_seq=C;Dbxref=dbSNP_129:rs53148771;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	deletion	16531	16531	.	+	.	ID=998;Variant_seq=-;Dbxref=dbSNP_129:rs53042754;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	16532	16532	.	+	.	ID=999;Variant_seq=T;Dbxref=dbSNP_129:rs52865062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	16642	16642	.	+	.	ID=1000;Variant_seq=A;Dbxref=dbSNP_129:rs54227340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398416.1	dbSNP	SNV	17649	17649	.	+	.	ID=1001;Variant_seq=T;Dbxref=dbSNP_129:rs53819958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	17659	17659	.	+	.	ID=1002;Variant_seq=A;Dbxref=dbSNP_129:rs53894296;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	17663	17663	.	+	.	ID=1003;Variant_seq=A;Dbxref=dbSNP_129:rs53818271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	17664	17664	.	+	.	ID=1004;Variant_seq=T;Dbxref=dbSNP_129:rs20171985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	17666	17666	.	+	.	ID=1005;Variant_seq=T;Dbxref=dbSNP_129:rs53199892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	17676	17676	.	+	.	ID=1006;Variant_seq=T;Dbxref=dbSNP_129:rs54223857;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398416.1	dbSNP	SNV	17686	17686	.	+	.	ID=1007;Variant_seq=A;Dbxref=dbSNP_129:rs53033593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398416.1	dbSNP	SNV	18485	18485	.	+	.	ID=1008;Variant_seq=C;Dbxref=dbSNP_129:rs20172525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048810.1	dbSNP	SNV	1162	1162	.	+	.	ID=1009;Variant_seq=A;Dbxref=dbSNP_129:rs19679650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048810.1	dbSNP	SNV	1191	1191	.	+	.	ID=1010;Variant_seq=G;Dbxref=dbSNP_129:rs19679630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048810.1	dbSNP	SNV	1221	1221	.	+	.	ID=1011;Variant_seq=C;Dbxref=dbSNP_129:rs19679620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048810.1	dbSNP	SNV	1365	1365	.	+	.	ID=1012;Variant_seq=A;Dbxref=dbSNP_129:rs19679610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048810.1	dbSNP	SNV	1370	1370	.	+	.	ID=1013;Variant_seq=A;Dbxref=dbSNP_129:rs19679600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048810.1	dbSNP	SNV	1377	1377	.	+	.	ID=1014;Variant_seq=T;Dbxref=dbSNP_129:rs19679590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048810.1	dbSNP	SNV	1540	1540	.	+	.	ID=1015;Variant_seq=C;Dbxref=dbSNP_129:rs19679560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399955.1	dbSNP	SNV	1240	1240	.	+	.	ID=1016;Variant_seq=G;Dbxref=dbSNP_129:rs21558394;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046787.1	dbSNP	SNV	1197	1197	.	+	.	ID=1017;Variant_seq=A;Dbxref=dbSNP_129:rs53404797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046787.1	dbSNP	SNV	1215	1215	.	+	.	ID=1018;Variant_seq=C;Dbxref=dbSNP_129:rs53205460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046787.1	dbSNP	SNV	1588	1588	.	+	.	ID=1019;Variant_seq=G;Dbxref=dbSNP_129:rs21585797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	674	674	.	+	.	ID=1020;Variant_seq=C;Dbxref=dbSNP_129:rs53176264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035774.1	dbSNP	SNV	676	676	.	+	.	ID=1021;Variant_seq=G;Dbxref=dbSNP_129:rs52916175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	1451	1451	.	+	.	ID=1022;Variant_seq=A;Dbxref=dbSNP_129:rs20175339;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035774.1	dbSNP	SNV	18553	18553	.	+	.	ID=1023;Variant_seq=T;Dbxref=dbSNP_129:rs18885008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035774.1	dbSNP	SNV	21834	21834	.	+	.	ID=1024;Variant_seq=T;Dbxref=dbSNP_129:rs18237285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035774.1	dbSNP	SNV	22559	22559	.	+	.	ID=1025;Variant_seq=A;Dbxref=dbSNP_129:rs18560849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035774.1	dbSNP	SNV	23486	23486	.	+	.	ID=1026;Variant_seq=C;Dbxref=dbSNP_129:rs20387105;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23487	23487	.	+	.	ID=1027;Variant_seq=G;Dbxref=dbSNP_129:rs20387115;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035774.1	dbSNP	SNV	23493	23493	.	+	.	ID=1028;Variant_seq=G;Dbxref=dbSNP_129:rs20387134;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23511	23511	.	+	.	ID=1029;Variant_seq=T;Dbxref=dbSNP_129:rs20387174;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23518	23518	.	+	.	ID=1030;Variant_seq=G;Dbxref=dbSNP_129:rs20387184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23519	23519	.	+	.	ID=1031;Variant_seq=C;Dbxref=dbSNP_129:rs20387194;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23520	23520	.	+	.	ID=1032;Variant_seq=G;Dbxref=dbSNP_129:rs20387204;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035774.1	dbSNP	SNV	23521	23521	.	+	.	ID=1033;Variant_seq=G;Dbxref=dbSNP_129:rs20387214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049569.1	dbSNP	SNV	1124	1124	.	+	.	ID=1034;Variant_seq=G;Dbxref=dbSNP_129:rs54108164;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049569.1	dbSNP	SNV	1656	1656	.	+	.	ID=1035;Variant_seq=A;Dbxref=dbSNP_129:rs53916125;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049569.1	dbSNP	SNV	1657	1657	.	+	.	ID=1036;Variant_seq=A;Dbxref=dbSNP_129:rs54287384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049569.1	dbSNP	SNV	1676	1676	.	+	.	ID=1037;Variant_seq=G;Dbxref=dbSNP_129:rs54320793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049569.1	dbSNP	SNV	1730	1730	.	+	.	ID=1038;Variant_seq=G;Dbxref=dbSNP_129:rs53406496;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399927.1	dbSNP	SNV	265	265	.	+	.	ID=1039;Variant_seq=G;Dbxref=dbSNP_129:rs21233927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399927.1	dbSNP	SNV	274	274	.	+	.	ID=1040;Variant_seq=G;Dbxref=dbSNP_129:rs21233917;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398491.1	dbSNP	SNV	316	316	.	+	.	ID=1041;Variant_seq=C;Dbxref=dbSNP_129:rs19039183;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	340	340	.	+	.	ID=1042;Variant_seq=C;Dbxref=dbSNP_129:rs19039203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	5446	5446	.	+	.	ID=1043;Variant_seq=G;Dbxref=dbSNP_129:rs21173440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398491.1	dbSNP	SNV	5457	5457	.	+	.	ID=1044;Variant_seq=C;Dbxref=dbSNP_129:rs21173430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	5458	5458	.	+	.	ID=1045;Variant_seq=A;Dbxref=dbSNP_129:rs21173420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	5472	5472	.	+	.	ID=1046;Variant_seq=A;Dbxref=dbSNP_129:rs21173400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	5473	5473	.	+	.	ID=1047;Variant_seq=A;Dbxref=dbSNP_129:rs21173390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	5484	5484	.	+	.	ID=1048;Variant_seq=C;Dbxref=dbSNP_129:rs21173370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	7008	7008	.	+	.	ID=1049;Variant_seq=A;Dbxref=dbSNP_129:rs53404797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	7026	7026	.	+	.	ID=1050;Variant_seq=C;Dbxref=dbSNP_129:rs53205460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	9441	9441	.	+	.	ID=1051;Variant_seq=T;Dbxref=dbSNP_129:rs21416971;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	9442	9442	.	+	.	ID=1052;Variant_seq=T;Dbxref=dbSNP_129:rs21416981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	9445	9445	.	+	.	ID=1053;Variant_seq=A;Dbxref=dbSNP_129:rs21416991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	9448	9448	.	+	.	ID=1054;Variant_seq=A;Dbxref=dbSNP_129:rs21417001;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	11823	11823	.	+	.	ID=1055;Variant_seq=T,G;Dbxref=dbSNP_129:rs53178111;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398491.1	dbSNP	SNV	11827	11827	.	+	.	ID=1056;Variant_seq=A;Dbxref=dbSNP_129:rs53685494;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	11828	11828	.	+	.	ID=1057;Variant_seq=A;Dbxref=dbSNP_129:rs52937284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	11830	11830	.	+	.	ID=1058;Variant_seq=G;Dbxref=dbSNP_129:rs54366818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398491.1	dbSNP	SNV	11831	11831	.	+	.	ID=1059;Variant_seq=T;Dbxref=dbSNP_129:rs53682663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	11832	11832	.	+	.	ID=1060;Variant_seq=C;Dbxref=dbSNP_129:rs54186947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	11833	11833	.	+	.	ID=1061;Variant_seq=C;Dbxref=dbSNP_129:rs53379936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	11834	11834	.	+	.	ID=1062;Variant_seq=A;Dbxref=dbSNP_129:rs53326957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	14293	14293	.	+	.	ID=1063;Variant_seq=A;Dbxref=dbSNP_129:rs19516218;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	14470	14470	.	+	.	ID=1064;Variant_seq=G;Dbxref=dbSNP_129:rs17918881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	14471	14471	.	+	.	ID=1065;Variant_seq=G;Dbxref=dbSNP_129:rs17918890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	14734	14734	.	+	.	ID=1066;Variant_seq=A;Dbxref=dbSNP_129:rs20641738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	14864	14864	.	+	.	ID=1067;Variant_seq=T;Dbxref=dbSNP_129:rs53157042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398491.1	dbSNP	SNV	14871	14871	.	+	.	ID=1068;Variant_seq=T;Dbxref=dbSNP_129:rs54154537;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398491.1	dbSNP	SNV	15363	15363	.	+	.	ID=1069;Variant_seq=A;Dbxref=dbSNP_129:rs21643428;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398491.1	dbSNP	SNV	15425	15425	.	+	.	ID=1070;Variant_seq=C;Dbxref=dbSNP_129:rs20579687;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043194.1	dbSNP	SNV	1474	1474	.	+	.	ID=1071;Variant_seq=A;Dbxref=dbSNP_129:rs17906391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043194.1	dbSNP	SNV	1876	1876	.	+	.	ID=1072;Variant_seq=C;Dbxref=dbSNP_129:rs20834913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043194.1	dbSNP	SNV	1877	1877	.	+	.	ID=1073;Variant_seq=C;Dbxref=dbSNP_129:rs20834923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043194.1	dbSNP	SNV	1885	1885	.	+	.	ID=1074;Variant_seq=A;Dbxref=dbSNP_129:rs20834933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043194.1	dbSNP	SNV	1897	1897	.	+	.	ID=1075;Variant_seq=C;Dbxref=dbSNP_129:rs20834983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043194.1	dbSNP	SNV	1910	1910	.	+	.	ID=1076;Variant_seq=G;Dbxref=dbSNP_129:rs20835013;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043194.1	dbSNP	SNV	1955	1955	.	+	.	ID=1077;Variant_seq=T;Dbxref=dbSNP_129:rs20835103;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043194.1	dbSNP	SNV	1967	1967	.	+	.	ID=1078;Variant_seq=T;Dbxref=dbSNP_129:rs20835163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	9302	9302	.	+	.	ID=1079;Variant_seq=G;Dbxref=dbSNP_129:rs21361397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	9312	9312	.	+	.	ID=1080;Variant_seq=A;Dbxref=dbSNP_129:rs20422081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	9868	9868	.	+	.	ID=1081;Variant_seq=T;Dbxref=dbSNP_129:rs19066760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10150	10150	.	+	.	ID=1082;Variant_seq=T;Dbxref=dbSNP_129:rs19066562;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10167	10167	.	+	.	ID=1083;Variant_seq=G;Dbxref=dbSNP_129:rs18878646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10221	10221	.	+	.	ID=1084;Variant_seq=C;Dbxref=dbSNP_129:rs19066483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10222	10222	.	+	.	ID=1085;Variant_seq=C;Dbxref=dbSNP_129:rs18878626;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10265	10265	.	+	.	ID=1086;Variant_seq=A;Dbxref=dbSNP_129:rs18878586;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10269	10269	.	+	.	ID=1087;Variant_seq=A;Dbxref=dbSNP_129:rs18878576;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10294	10294	.	+	.	ID=1088;Variant_seq=A;Dbxref=dbSNP_129:rs18878566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10296	10296	.	+	.	ID=1089;Variant_seq=C;Dbxref=dbSNP_129:rs18878556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	10347	10347	.	+	.	ID=1090;Variant_seq=C;Dbxref=dbSNP_129:rs18878536;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10370	10370	.	+	.	ID=1091;Variant_seq=A;Dbxref=dbSNP_129:rs18878526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	10371	10371	.	+	.	ID=1092;Variant_seq=A;Dbxref=dbSNP_129:rs18878516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10379	10379	.	+	.	ID=1093;Variant_seq=T;Dbxref=dbSNP_129:rs18878506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10389	10389	.	+	.	ID=1094;Variant_seq=T;Dbxref=dbSNP_129:rs17906511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10390	10390	.	+	.	ID=1095;Variant_seq=A;Dbxref=dbSNP_129:rs17906512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10399	10399	.	+	.	ID=1096;Variant_seq=A;Dbxref=dbSNP_129:rs18878486;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10403	10403	.	+	.	ID=1097;Variant_seq=G;Dbxref=dbSNP_129:rs18878476;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10410	10410	.	+	.	ID=1098;Variant_seq=T;Dbxref=dbSNP_129:rs18878466;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10444	10444	.	+	.	ID=1099;Variant_seq=G;Dbxref=dbSNP_129:rs19066063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10458	10458	.	+	.	ID=1100;Variant_seq=A;Dbxref=dbSNP_129:rs18878446;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10461	10461	.	+	.	ID=1101;Variant_seq=G;Dbxref=dbSNP_129:rs18878426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10474	10474	.	+	.	ID=1102;Variant_seq=T;Dbxref=dbSNP_129:rs18878416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10475	10475	.	+	.	ID=1103;Variant_seq=G;Dbxref=dbSNP_129:rs18878406;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10481	10481	.	+	.	ID=1104;Variant_seq=T;Dbxref=dbSNP_129:rs18878396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10483	10483	.	+	.	ID=1105;Variant_seq=G;Dbxref=dbSNP_129:rs18878386;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10497	10497	.	+	.	ID=1106;Variant_seq=A;Dbxref=dbSNP_129:rs18878366;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10502	10502	.	+	.	ID=1107;Variant_seq=A;Dbxref=dbSNP_129:rs18878356;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	10525	10525	.	+	.	ID=1108;Variant_seq=A;Dbxref=dbSNP_129:rs18878346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10527	10527	.	+	.	ID=1109;Variant_seq=G;Dbxref=dbSNP_129:rs18878336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10529	10529	.	+	.	ID=1110;Variant_seq=A;Dbxref=dbSNP_129:rs18878326;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	10545	10545	.	+	.	ID=1111;Variant_seq=T;Dbxref=dbSNP_129:rs19065773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10552	10552	.	+	.	ID=1112;Variant_seq=C;Dbxref=dbSNP_129:rs19065724;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10557	10557	.	+	.	ID=1113;Variant_seq=G;Dbxref=dbSNP_129:rs18878306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10572	10572	.	+	.	ID=1114;Variant_seq=A;Dbxref=dbSNP_129:rs18878296;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	10790	10790	.	+	.	ID=1115;Variant_seq=T;Dbxref=dbSNP_129:rs19065247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	10859	10859	.	+	.	ID=1116;Variant_seq=T;Dbxref=dbSNP_129:rs18878236;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	10989	10989	.	+	.	ID=1117;Variant_seq=A;Dbxref=dbSNP_129:rs18878156;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	11009	11009	.	+	.	ID=1118;Variant_seq=G;Dbxref=dbSNP_129:rs18878146;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	12660	12660	.	+	.	ID=1119;Variant_seq=T;Dbxref=dbSNP_129:rs53637164;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	17591	17591	.	+	.	ID=1120;Variant_seq=G;Dbxref=dbSNP_129:rs52974587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	18483	18483	.	+	.	ID=1121;Variant_seq=G;Dbxref=dbSNP_129:rs19067150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	18490	18490	.	+	.	ID=1122;Variant_seq=A;Dbxref=dbSNP_129:rs19067140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	18492	18492	.	+	.	ID=1123;Variant_seq=A;Dbxref=dbSNP_129:rs19067130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	18495	18495	.	+	.	ID=1124;Variant_seq=A;Dbxref=dbSNP_129:rs19067120;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	18499	18499	.	+	.	ID=1125;Variant_seq=T;Dbxref=dbSNP_129:rs19067110;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	18507	18507	.	+	.	ID=1126;Variant_seq=A;Dbxref=dbSNP_129:rs19067100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	18516	18516	.	+	.	ID=1127;Variant_seq=T;Dbxref=dbSNP_129:rs19067080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	18519	18519	.	+	.	ID=1128;Variant_seq=C;Dbxref=dbSNP_129:rs19067070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	18525	18525	.	+	.	ID=1129;Variant_seq=T;Dbxref=dbSNP_129:rs19067060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036388.1	dbSNP	SNV	18528	18528	.	+	.	ID=1130;Variant_seq=C;Dbxref=dbSNP_129:rs19067050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	18543	18543	.	+	.	ID=1131;Variant_seq=G;Dbxref=dbSNP_129:rs19067040;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	18564	18564	.	+	.	ID=1132;Variant_seq=C;Dbxref=dbSNP_129:rs19067010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	18591	18591	.	+	.	ID=1133;Variant_seq=T;Dbxref=dbSNP_129:rs19066990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036388.1	dbSNP	SNV	18616	18616	.	+	.	ID=1134;Variant_seq=G;Dbxref=dbSNP_129:rs19066970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036388.1	dbSNP	SNV	18621	18621	.	+	.	ID=1135;Variant_seq=C;Dbxref=dbSNP_129:rs19066960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036388.1	dbSNP	SNV	18625	18625	.	+	.	ID=1136;Variant_seq=C;Dbxref=dbSNP_129:rs19066950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398794.1	dbSNP	SNV	167	167	.	+	.	ID=1137;Variant_seq=A;Dbxref=dbSNP_129:rs20654399;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043473.1	dbSNP	SNV	2174	2174	.	+	.	ID=1138;Variant_seq=G;Dbxref=dbSNP_129:rs53697941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043473.1	dbSNP	SNV	2178	2178	.	+	.	ID=1139;Variant_seq=A;Dbxref=dbSNP_129:rs53103459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043473.1	dbSNP	SNV	2179	2179	.	+	.	ID=1140;Variant_seq=C;Dbxref=dbSNP_129:rs54390348;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043473.1	dbSNP	SNV	2212	2212	.	+	.	ID=1141;Variant_seq=A;Dbxref=dbSNP_129:rs54373364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043473.1	dbSNP	SNV	2546	2546	.	+	.	ID=1142;Variant_seq=C;Dbxref=dbSNP_129:rs18775843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399789.1	dbSNP	SNV	4175	4175	.	+	.	ID=1143;Variant_seq=A;Dbxref=dbSNP_129:rs53694086;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401121.1	dbSNP	SNV	1787	1787	.	+	.	ID=1144;Variant_seq=C;Dbxref=dbSNP_129:rs21752517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401121.1	dbSNP	SNV	1884	1884	.	+	.	ID=1145;Variant_seq=C;Dbxref=dbSNP_129:rs21752526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401121.1	dbSNP	SNV	1885	1885	.	+	.	ID=1146;Variant_seq=A;Dbxref=dbSNP_129:rs21752535;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401121.1	dbSNP	SNV	1886	1886	.	+	.	ID=1147;Variant_seq=T;Dbxref=dbSNP_129:rs21752544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401121.1	dbSNP	SNV	1887	1887	.	+	.	ID=1148;Variant_seq=A;Dbxref=dbSNP_129:rs21752553;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401121.1	dbSNP	SNV	1888	1888	.	+	.	ID=1149;Variant_seq=G;Dbxref=dbSNP_129:rs21752562;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401121.1	dbSNP	SNV	1891	1891	.	+	.	ID=1150;Variant_seq=G;Dbxref=dbSNP_129:rs21752571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401121.1	dbSNP	SNV	1895	1895	.	+	.	ID=1151;Variant_seq=G;Dbxref=dbSNP_129:rs21752580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	375	375	.	+	.	ID=1152;Variant_seq=G;Dbxref=dbSNP_129:rs53700027;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	418	418	.	+	.	ID=1153;Variant_seq=C;Dbxref=dbSNP_129:rs20670228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	441	441	.	+	.	ID=1154;Variant_seq=A;Dbxref=dbSNP_129:rs19404824;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	486	486	.	+	.	ID=1155;Variant_seq=T;Dbxref=dbSNP_129:rs53704512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	1236	1236	.	+	.	ID=1156;Variant_seq=T;Dbxref=dbSNP_129:rs21359736;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	1962	1962	.	+	.	ID=1157;Variant_seq=T;Dbxref=dbSNP_129:rs19404624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	2736	2736	.	+	.	ID=1158;Variant_seq=T;Dbxref=dbSNP_129:rs53459413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	2737	2737	.	+	.	ID=1159;Variant_seq=T;Dbxref=dbSNP_129:rs54260070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	3107	3107	.	+	.	ID=1160;Variant_seq=G;Dbxref=dbSNP_129:rs21360136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	3363	3363	.	+	.	ID=1161;Variant_seq=C;Dbxref=dbSNP_129:rs21209064;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	3363	3363	.	+	.	ID=1162;Variant_seq=C;Dbxref=dbSNP_129:rs53224328;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	7581	7581	.	+	.	ID=1163;Variant_seq=A;Dbxref=dbSNP_129:rs18416162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	7619	7619	.	+	.	ID=1164;Variant_seq=T;Dbxref=dbSNP_129:rs18416144;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	7791	7791	.	+	.	ID=1165;Variant_seq=A;Dbxref=dbSNP_129:rs20669299;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	8561	8561	.	+	.	ID=1166;Variant_seq=A;Dbxref=dbSNP_129:rs53268668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	8925	8925	.	+	.	ID=1167;Variant_seq=T;Dbxref=dbSNP_129:rs18710735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	11877	11877	.	+	.	ID=1168;Variant_seq=A;Dbxref=dbSNP_129:rs19499691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	11878	11878	.	+	.	ID=1169;Variant_seq=T;Dbxref=dbSNP_129:rs19499701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	11879	11879	.	+	.	ID=1170;Variant_seq=C;Dbxref=dbSNP_129:rs19499711;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	insertion	11954	11954	.	+	.	ID=1171;Variant_seq=CGTACTATAACAT;Dbxref=dbSNP_129:rs54060409;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02036132.1	dbSNP	SNV	12112	12112	.	+	.	ID=1172;Variant_seq=A;Dbxref=dbSNP_129:rs18129566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	12116	12116	.	+	.	ID=1173;Variant_seq=T;Dbxref=dbSNP_129:rs53882669;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	12160	12160	.	+	.	ID=1174;Variant_seq=G;Dbxref=dbSNP_129:rs54316800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12176	12176	.	+	.	ID=1175;Variant_seq=C;Dbxref=dbSNP_129:rs19500771;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12181	12181	.	+	.	ID=1176;Variant_seq=G;Dbxref=dbSNP_129:rs19500781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036132.1	dbSNP	SNV	12188	12188	.	+	.	ID=1177;Variant_seq=C;Dbxref=dbSNP_129:rs19500801;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	12191	12191	.	+	.	ID=1178;Variant_seq=T;Dbxref=dbSNP_129:rs19500811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12195	12195	.	+	.	ID=1179;Variant_seq=C;Dbxref=dbSNP_129:rs19500831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12197	12197	.	+	.	ID=1180;Variant_seq=T;Dbxref=dbSNP_129:rs19500841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036132.1	dbSNP	SNV	12201	12201	.	+	.	ID=1181;Variant_seq=C;Dbxref=dbSNP_129:rs19500863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12214	12214	.	+	.	ID=1182;Variant_seq=C;Dbxref=dbSNP_129:rs19500883;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12220	12220	.	+	.	ID=1183;Variant_seq=C;Dbxref=dbSNP_129:rs19500903;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	12221	12221	.	+	.	ID=1184;Variant_seq=A;Dbxref=dbSNP_129:rs19500913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	12269	12269	.	+	.	ID=1185;Variant_seq=G;Dbxref=dbSNP_129:rs20034702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036132.1	dbSNP	SNV	12314	12314	.	+	.	ID=1186;Variant_seq=G;Dbxref=dbSNP_129:rs19501393;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036132.1	dbSNP	SNV	14813	14813	.	+	.	ID=1187;Variant_seq=T;Dbxref=dbSNP_129:rs18521662;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040399.1	dbSNP	SNV	1385	1385	.	+	.	ID=1188;Variant_seq=C;Dbxref=dbSNP_129:rs20688940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398876.1	dbSNP	SNV	8772	8772	.	+	.	ID=1189;Variant_seq=C;Dbxref=dbSNP_129:rs19105683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044875.1	dbSNP	SNV	2230	2230	.	+	.	ID=1190;Variant_seq=A;Dbxref=dbSNP_129:rs21464947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039867.1	dbSNP	SNV	4393	4393	.	+	.	ID=1191;Variant_seq=G;Dbxref=dbSNP_129:rs17896658;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400974.1	dbSNP	SNV	1552	1552	.	+	.	ID=1192;Variant_seq=A;Dbxref=dbSNP_129:rs21369201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400974.1	dbSNP	SNV	1553	1553	.	+	.	ID=1193;Variant_seq=T;Dbxref=dbSNP_129:rs21369191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400974.1	dbSNP	SNV	1556	1556	.	+	.	ID=1194;Variant_seq=A;Dbxref=dbSNP_129:rs21369181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400974.1	dbSNP	SNV	1588	1588	.	+	.	ID=1195;Variant_seq=C;Dbxref=dbSNP_129:rs21369171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043747.1	dbSNP	SNV	1147	1147	.	+	.	ID=1196;Variant_seq=T;Dbxref=dbSNP_129:rs53226243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043747.1	dbSNP	SNV	1162	1162	.	+	.	ID=1197;Variant_seq=A;Dbxref=dbSNP_129:rs54260445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041110.1	dbSNP	SNV	378	378	.	+	.	ID=1198;Variant_seq=G;Dbxref=dbSNP_129:rs53498604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041110.1	dbSNP	SNV	380	380	.	+	.	ID=1199;Variant_seq=A;Dbxref=dbSNP_129:rs53520365;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041110.1	dbSNP	SNV	396	396	.	+	.	ID=1200;Variant_seq=G;Dbxref=dbSNP_129:rs54297038;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041110.1	dbSNP	SNV	399	399	.	+	.	ID=1201;Variant_seq=A;Dbxref=dbSNP_129:rs53053869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041110.1	dbSNP	SNV	403	403	.	+	.	ID=1202;Variant_seq=G;Dbxref=dbSNP_129:rs52884156;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041110.1	dbSNP	SNV	410	410	.	+	.	ID=1203;Variant_seq=C;Dbxref=dbSNP_129:rs20033452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041110.1	dbSNP	SNV	3311	3311	.	+	.	ID=1204;Variant_seq=A;Dbxref=dbSNP_129:rs20736987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041110.1	dbSNP	SNV	3325	3325	.	+	.	ID=1205;Variant_seq=G;Dbxref=dbSNP_129:rs20736967;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041110.1	dbSNP	SNV	3328	3328	.	+	.	ID=1206;Variant_seq=C;Dbxref=dbSNP_129:rs20736957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041110.1	dbSNP	SNV	4373	4373	.	+	.	ID=1207;Variant_seq=A;Dbxref=dbSNP_129:rs20033412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398847.1	dbSNP	SNV	3494	3494	.	+	.	ID=1208;Variant_seq=T;Dbxref=dbSNP_129:rs53805933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398847.1	dbSNP	SNV	6169	6169	.	+	.	ID=1209;Variant_seq=A;Dbxref=dbSNP_129:rs53455681;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398847.1	dbSNP	SNV	6171	6171	.	+	.	ID=1210;Variant_seq=A;Dbxref=dbSNP_129:rs53657303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398847.1	dbSNP	SNV	6172	6172	.	+	.	ID=1211;Variant_seq=T;Dbxref=dbSNP_129:rs53530231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398847.1	dbSNP	SNV	6178	6178	.	+	.	ID=1212;Variant_seq=A,C;Dbxref=dbSNP_129:rs54252294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398847.1	dbSNP	SNV	6181	6181	.	+	.	ID=1213;Variant_seq=A;Dbxref=dbSNP_129:rs52966988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398847.1	dbSNP	SNV	8720	8720	.	+	.	ID=1214;Variant_seq=A;Dbxref=dbSNP_129:rs21475374;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398847.1	dbSNP	SNV	8963	8963	.	+	.	ID=1215;Variant_seq=C;Dbxref=dbSNP_129:rs21475664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398847.1	dbSNP	SNV	8974	8974	.	+	.	ID=1216;Variant_seq=G;Dbxref=dbSNP_129:rs21475684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044441.1	dbSNP	SNV	448	448	.	+	.	ID=1217;Variant_seq=T;Dbxref=dbSNP_129:rs53822578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044441.1	dbSNP	SNV	449	449	.	+	.	ID=1218;Variant_seq=G;Dbxref=dbSNP_129:rs54173061;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044441.1	dbSNP	SNV	2163	2163	.	+	.	ID=1219;Variant_seq=T;Dbxref=dbSNP_129:rs19221068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038749.1	dbSNP	SNV	612	612	.	+	.	ID=1220;Variant_seq=A;Dbxref=dbSNP_129:rs18256025;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038749.1	dbSNP	SNV	2678	2678	.	+	.	ID=1221;Variant_seq=C;Dbxref=dbSNP_129:rs19175790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038749.1	dbSNP	SNV	6180	6180	.	+	.	ID=1222;Variant_seq=T;Dbxref=dbSNP_129:rs53655195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038749.1	dbSNP	SNV	7006	7006	.	+	.	ID=1223;Variant_seq=A;Dbxref=dbSNP_129:rs20139013;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038749.1	dbSNP	SNV	7114	7114	.	+	.	ID=1224;Variant_seq=T;Dbxref=dbSNP_129:rs21504451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039187.1	dbSNP	SNV	914	914	.	+	.	ID=1225;Variant_seq=T;Dbxref=dbSNP_129:rs53190608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039187.1	dbSNP	SNV	2629	2629	.	+	.	ID=1226;Variant_seq=A;Dbxref=dbSNP_129:rs21602732;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039187.1	dbSNP	SNV	6242	6242	.	+	.	ID=1227;Variant_seq=C;Dbxref=dbSNP_129:rs21556995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399919.1	dbSNP	SNV	1624	1624	.	+	.	ID=1228;Variant_seq=T;Dbxref=dbSNP_129:rs18770956;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	1985	1985	.	+	.	ID=1229;Variant_seq=G;Dbxref=dbSNP_129:rs53525924;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2030	2030	.	+	.	ID=1230;Variant_seq=C;Dbxref=dbSNP_129:rs54250542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2031	2031	.	+	.	ID=1231;Variant_seq=A;Dbxref=dbSNP_129:rs53152550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2032	2032	.	+	.	ID=1232;Variant_seq=C;Dbxref=dbSNP_129:rs54011715;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2039	2039	.	+	.	ID=1233;Variant_seq=G;Dbxref=dbSNP_129:rs53118609;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2073	2073	.	+	.	ID=1234;Variant_seq=C;Dbxref=dbSNP_129:rs53545606;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2116	2116	.	+	.	ID=1235;Variant_seq=G;Dbxref=dbSNP_129:rs53805030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2158	2158	.	+	.	ID=1236;Variant_seq=T;Dbxref=dbSNP_129:rs54174584;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2166	2166	.	+	.	ID=1237;Variant_seq=T;Dbxref=dbSNP_129:rs53290709;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2188	2188	.	+	.	ID=1238;Variant_seq=C;Dbxref=dbSNP_129:rs53139852;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2200	2200	.	+	.	ID=1239;Variant_seq=T;Dbxref=dbSNP_129:rs53714255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2211	2211	.	+	.	ID=1240;Variant_seq=T;Dbxref=dbSNP_129:rs53252093;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2214	2214	.	+	.	ID=1241;Variant_seq=C;Dbxref=dbSNP_129:rs54263247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2217	2217	.	+	.	ID=1242;Variant_seq=A;Dbxref=dbSNP_129:rs53981342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2223	2223	.	+	.	ID=1243;Variant_seq=A;Dbxref=dbSNP_129:rs53754421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	deletion	2226	2226	.	+	.	ID=1244;Variant_seq=-;Dbxref=dbSNP_129:rs52980989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2231	2231	.	+	.	ID=1245;Variant_seq=C;Dbxref=dbSNP_129:rs53424680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2233	2233	.	+	.	ID=1246;Variant_seq=A;Dbxref=dbSNP_129:rs54231524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	insertion	2240	2240	.	+	.	ID=1247;Variant_seq=A;Dbxref=dbSNP_129:rs52935362;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02041850.1	dbSNP	SNV	2243	2243	.	+	.	ID=1248;Variant_seq=T;Dbxref=dbSNP_129:rs53474108;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	insertion	2254	2254	.	+	.	ID=1249;Variant_seq=GATTAATAAT;Dbxref=dbSNP_129:rs54281841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02041850.1	dbSNP	SNV	2256	2256	.	+	.	ID=1250;Variant_seq=A;Dbxref=dbSNP_129:rs52918089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2260	2260	.	+	.	ID=1251;Variant_seq=G;Dbxref=dbSNP_129:rs54191287;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2262	2262	.	+	.	ID=1252;Variant_seq=G;Dbxref=dbSNP_129:rs53019605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2270	2270	.	+	.	ID=1253;Variant_seq=G;Dbxref=dbSNP_129:rs53625258;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2283	2283	.	+	.	ID=1254;Variant_seq=T;Dbxref=dbSNP_129:rs52949720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2284	2284	.	+	.	ID=1255;Variant_seq=G;Dbxref=dbSNP_129:rs54129891;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2294	2294	.	+	.	ID=1256;Variant_seq=T;Dbxref=dbSNP_129:rs54365342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2297	2297	.	+	.	ID=1257;Variant_seq=G;Dbxref=dbSNP_129:rs53517376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	deletion	2299	2299	.	+	.	ID=1258;Variant_seq=-;Dbxref=dbSNP_129:rs54136837;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2302	2302	.	+	.	ID=1259;Variant_seq=C;Dbxref=dbSNP_129:rs53193349;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2303	2303	.	+	.	ID=1260;Variant_seq=C;Dbxref=dbSNP_129:rs53492310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2312	2312	.	+	.	ID=1261;Variant_seq=A;Dbxref=dbSNP_129:rs54331973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2322	2322	.	+	.	ID=1262;Variant_seq=G;Dbxref=dbSNP_129:rs54052516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	deletion	2331	2335	.	+	.	ID=1263;Variant_seq=-;Dbxref=dbSNP_129:rs52865599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TAAAT
AAAA02041850.1	dbSNP	SNV	2342	2342	.	+	.	ID=1264;Variant_seq=A;Dbxref=dbSNP_129:rs54134930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2344	2344	.	+	.	ID=1265;Variant_seq=T;Dbxref=dbSNP_129:rs53791448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	SNV	2349	2349	.	+	.	ID=1266;Variant_seq=C;Dbxref=dbSNP_129:rs53648435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2364	2364	.	+	.	ID=1267;Variant_seq=C;Dbxref=dbSNP_129:rs54194176;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2365	2365	.	+	.	ID=1268;Variant_seq=T;Dbxref=dbSNP_129:rs53897874;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041850.1	dbSNP	deletion	2369	2373	.	+	.	ID=1269;Variant_seq=-;Dbxref=dbSNP_129:rs53377960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AAAAT
AAAA02041850.1	dbSNP	deletion	2380	2382	.	+	.	ID=1270;Variant_seq=-;Dbxref=dbSNP_129:rs53345900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=GAA
AAAA02041850.1	dbSNP	insertion	2382	2382	.	+	.	ID=1271;Variant_seq=TAAAA;Dbxref=dbSNP_129:rs53823021;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02041850.1	dbSNP	SNV	2386	2386	.	+	.	ID=1272;Variant_seq=A;Dbxref=dbSNP_129:rs53307286;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2387	2387	.	+	.	ID=1273;Variant_seq=A;Dbxref=dbSNP_129:rs54080783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2391	2391	.	+	.	ID=1274;Variant_seq=T;Dbxref=dbSNP_129:rs53569807;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2393	2393	.	+	.	ID=1275;Variant_seq=C;Dbxref=dbSNP_129:rs54084949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2396	2396	.	+	.	ID=1276;Variant_seq=C;Dbxref=dbSNP_129:rs52901862;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	2406	2406	.	+	.	ID=1277;Variant_seq=C;Dbxref=dbSNP_129:rs53491100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2416	2416	.	+	.	ID=1278;Variant_seq=C;Dbxref=dbSNP_129:rs53814965;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2427	2427	.	+	.	ID=1279;Variant_seq=C;Dbxref=dbSNP_129:rs54091755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041850.1	dbSNP	SNV	2429	2429	.	+	.	ID=1280;Variant_seq=A;Dbxref=dbSNP_129:rs53864666;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041850.1	dbSNP	SNV	2431	2431	.	+	.	ID=1281;Variant_seq=G;Dbxref=dbSNP_129:rs53656316;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041850.1	dbSNP	SNV	3394	3394	.	+	.	ID=1282;Variant_seq=T;Dbxref=dbSNP_129:rs19019892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049524.1	dbSNP	SNV	638	638	.	+	.	ID=1283;Variant_seq=T;Dbxref=dbSNP_129:rs18575351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399923.1	dbSNP	SNV	1006	1006	.	+	.	ID=1284;Variant_seq=G;Dbxref=dbSNP_129:rs53651097;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400845.1	dbSNP	SNV	303	303	.	+	.	ID=1285;Variant_seq=G;Dbxref=dbSNP_129:rs19072778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400845.1	dbSNP	SNV	1294	1294	.	+	.	ID=1286;Variant_seq=A;Dbxref=dbSNP_129:rs18177697;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400845.1	dbSNP	SNV	2278	2278	.	+	.	ID=1287;Variant_seq=C;Dbxref=dbSNP_129:rs21613892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400845.1	dbSNP	SNV	2284	2284	.	+	.	ID=1288;Variant_seq=T;Dbxref=dbSNP_129:rs21613901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400845.1	dbSNP	SNV	2294	2294	.	+	.	ID=1289;Variant_seq=T;Dbxref=dbSNP_129:rs21613910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	167	167	.	+	.	ID=1290;Variant_seq=C;Dbxref=dbSNP_129:rs53619540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	169	169	.	+	.	ID=1291;Variant_seq=G;Dbxref=dbSNP_129:rs21328816;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	175	175	.	+	.	ID=1292;Variant_seq=G;Dbxref=dbSNP_129:rs54023374;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048233.1	dbSNP	SNV	182	182	.	+	.	ID=1293;Variant_seq=T;Dbxref=dbSNP_129:rs53915938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	183	183	.	+	.	ID=1294;Variant_seq=T;Dbxref=dbSNP_129:rs53717941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	185	185	.	+	.	ID=1295;Variant_seq=T;Dbxref=dbSNP_129:rs53553566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	217	217	.	+	.	ID=1296;Variant_seq=C;Dbxref=dbSNP_129:rs21328886;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	235	235	.	+	.	ID=1297;Variant_seq=C;Dbxref=dbSNP_129:rs53924787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	244	244	.	+	.	ID=1298;Variant_seq=A;Dbxref=dbSNP_129:rs53851336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	250	250	.	+	.	ID=1299;Variant_seq=C;Dbxref=dbSNP_129:rs21328946;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	259	259	.	+	.	ID=1300;Variant_seq=A;Dbxref=dbSNP_129:rs54014645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	271	271	.	+	.	ID=1301;Variant_seq=G;Dbxref=dbSNP_129:rs53370189;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048233.1	dbSNP	SNV	272	272	.	+	.	ID=1302;Variant_seq=A;Dbxref=dbSNP_129:rs53902006;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	284	284	.	+	.	ID=1303;Variant_seq=T;Dbxref=dbSNP_129:rs53636230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	286	286	.	+	.	ID=1304;Variant_seq=A;Dbxref=dbSNP_129:rs54128004;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	289	289	.	+	.	ID=1305;Variant_seq=G;Dbxref=dbSNP_129:rs52952084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048233.1	dbSNP	SNV	292	292	.	+	.	ID=1306;Variant_seq=T;Dbxref=dbSNP_129:rs53408227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	306	306	.	+	.	ID=1307;Variant_seq=A;Dbxref=dbSNP_129:rs54164397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	307	307	.	+	.	ID=1308;Variant_seq=A;Dbxref=dbSNP_129:rs53475005;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	313	313	.	+	.	ID=1309;Variant_seq=G;Dbxref=dbSNP_129:rs54190311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048233.1	dbSNP	SNV	316	316	.	+	.	ID=1310;Variant_seq=A;Dbxref=dbSNP_129:rs53599178;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	334	334	.	+	.	ID=1311;Variant_seq=A;Dbxref=dbSNP_129:rs53851099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	337	337	.	+	.	ID=1312;Variant_seq=A;Dbxref=dbSNP_129:rs52979424;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	373	373	.	+	.	ID=1313;Variant_seq=A;Dbxref=dbSNP_129:rs54044810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	394	394	.	+	.	ID=1314;Variant_seq=T;Dbxref=dbSNP_129:rs52911689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	402	402	.	+	.	ID=1315;Variant_seq=C;Dbxref=dbSNP_129:rs53232526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	408	408	.	+	.	ID=1316;Variant_seq=G;Dbxref=dbSNP_129:rs53356098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	deletion	413	416	.	+	.	ID=1317;Variant_seq=-;Dbxref=dbSNP_129:rs53232502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=GATC
AAAA02048233.1	dbSNP	SNV	415	415	.	+	.	ID=1318;Variant_seq=A;Dbxref=dbSNP_129:rs53705308;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	421	421	.	+	.	ID=1319;Variant_seq=T;Dbxref=dbSNP_129:rs54109187;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	426	426	.	+	.	ID=1320;Variant_seq=A;Dbxref=dbSNP_129:rs53711135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	427	427	.	+	.	ID=1321;Variant_seq=T;Dbxref=dbSNP_129:rs53395403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	433	433	.	+	.	ID=1322;Variant_seq=G;Dbxref=dbSNP_129:rs52903759;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	442	442	.	+	.	ID=1323;Variant_seq=A;Dbxref=dbSNP_129:rs54117371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048233.1	dbSNP	SNV	451	451	.	+	.	ID=1324;Variant_seq=C;Dbxref=dbSNP_129:rs53855452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	453	453	.	+	.	ID=1325;Variant_seq=C;Dbxref=dbSNP_129:rs52889174;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	461	461	.	+	.	ID=1326;Variant_seq=C;Dbxref=dbSNP_129:rs53894004;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048233.1	dbSNP	SNV	473	473	.	+	.	ID=1327;Variant_seq=A;Dbxref=dbSNP_129:rs53195515;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	489	489	.	+	.	ID=1328;Variant_seq=A;Dbxref=dbSNP_129:rs54185462;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048233.1	dbSNP	SNV	492	492	.	+	.	ID=1329;Variant_seq=G;Dbxref=dbSNP_129:rs53371491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048233.1	dbSNP	SNV	495	495	.	+	.	ID=1330;Variant_seq=A;Dbxref=dbSNP_129:rs53553458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040688.1	dbSNP	SNV	1248	1248	.	+	.	ID=1331;Variant_seq=A;Dbxref=dbSNP_129:rs19376181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040688.1	dbSNP	SNV	1249	1249	.	+	.	ID=1332;Variant_seq=C;Dbxref=dbSNP_129:rs19376191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040688.1	dbSNP	SNV	3153	3153	.	+	.	ID=1333;Variant_seq=T;Dbxref=dbSNP_129:rs20273469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042589.1	dbSNP	SNV	3677	3677	.	+	.	ID=1334;Variant_seq=C;Dbxref=dbSNP_129:rs19975435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041042.1	dbSNP	SNV	4319	4319	.	+	.	ID=1335;Variant_seq=C;Dbxref=dbSNP_129:rs20685145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041042.1	dbSNP	SNV	4369	4369	.	+	.	ID=1336;Variant_seq=C;Dbxref=dbSNP_129:rs20685135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041042.1	dbSNP	SNV	4371	4371	.	+	.	ID=1337;Variant_seq=G;Dbxref=dbSNP_129:rs20685125;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399005.1	dbSNP	SNV	2135	2135	.	+	.	ID=1338;Variant_seq=T;Dbxref=dbSNP_129:rs53452596;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399005.1	dbSNP	SNV	4005	4005	.	+	.	ID=1339;Variant_seq=A;Dbxref=dbSNP_129:rs20452809;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399005.1	dbSNP	SNV	4395	4395	.	+	.	ID=1340;Variant_seq=C;Dbxref=dbSNP_129:rs20728371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399005.1	dbSNP	SNV	4499	4499	.	+	.	ID=1341;Variant_seq=T;Dbxref=dbSNP_129:rs20452699;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399005.1	dbSNP	SNV	7762	7762	.	+	.	ID=1342;Variant_seq=C;Dbxref=dbSNP_129:rs18671307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399005.1	dbSNP	SNV	7786	7786	.	+	.	ID=1343;Variant_seq=G;Dbxref=dbSNP_129:rs18671334;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040462.1	dbSNP	SNV	584	584	.	+	.	ID=1344;Variant_seq=G;Dbxref=dbSNP_129:rs19539830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040462.1	dbSNP	SNV	602	602	.	+	.	ID=1345;Variant_seq=G;Dbxref=dbSNP_129:rs19539820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040462.1	dbSNP	SNV	3566	3566	.	+	.	ID=1346;Variant_seq=A;Dbxref=dbSNP_129:rs19806232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040462.1	dbSNP	SNV	3804	3804	.	+	.	ID=1347;Variant_seq=A;Dbxref=dbSNP_129:rs20872425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040462.1	dbSNP	SNV	3805	3805	.	+	.	ID=1348;Variant_seq=G;Dbxref=dbSNP_129:rs20872435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040462.1	dbSNP	SNV	3808	3808	.	+	.	ID=1349;Variant_seq=C;Dbxref=dbSNP_129:rs20872445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040462.1	dbSNP	SNV	3810	3810	.	+	.	ID=1350;Variant_seq=A;Dbxref=dbSNP_129:rs20872455;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040462.1	dbSNP	SNV	3813	3813	.	+	.	ID=1351;Variant_seq=T;Dbxref=dbSNP_129:rs20872465;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040462.1	dbSNP	SNV	3814	3814	.	+	.	ID=1352;Variant_seq=T;Dbxref=dbSNP_129:rs20872475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040462.1	dbSNP	SNV	3857	3857	.	+	.	ID=1353;Variant_seq=T;Dbxref=dbSNP_129:rs20872585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399809.1	dbSNP	SNV	1546	1546	.	+	.	ID=1354;Variant_seq=A;Dbxref=dbSNP_129:rs54113138;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399809.1	dbSNP	SNV	1922	1922	.	+	.	ID=1355;Variant_seq=T;Dbxref=dbSNP_129:rs54260795;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400005.1	dbSNP	SNV	2145	2145	.	+	.	ID=1356;Variant_seq=C;Dbxref=dbSNP_129:rs20850502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400005.1	dbSNP	SNV	2165	2165	.	+	.	ID=1357;Variant_seq=C;Dbxref=dbSNP_129:rs20850452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400005.1	dbSNP	SNV	2166	2166	.	+	.	ID=1358;Variant_seq=A;Dbxref=dbSNP_129:rs20850442;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400005.1	dbSNP	SNV	2174	2174	.	+	.	ID=1359;Variant_seq=T;Dbxref=dbSNP_129:rs53464927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	191	191	.	+	.	ID=1360;Variant_seq=C;Dbxref=dbSNP_129:rs18270937;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047407.1	dbSNP	SNV	218	218	.	+	.	ID=1361;Variant_seq=A;Dbxref=dbSNP_129:rs18270946;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047407.1	dbSNP	SNV	390	390	.	+	.	ID=1362;Variant_seq=T;Dbxref=dbSNP_129:rs18270964;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	424	424	.	+	.	ID=1363;Variant_seq=T;Dbxref=dbSNP_129:rs18270982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	516	516	.	+	.	ID=1364;Variant_seq=T;Dbxref=dbSNP_129:rs18270991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	691	691	.	+	.	ID=1365;Variant_seq=T;Dbxref=dbSNP_129:rs18271009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	707	707	.	+	.	ID=1366;Variant_seq=C;Dbxref=dbSNP_129:rs18271018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047407.1	dbSNP	SNV	775	775	.	+	.	ID=1367;Variant_seq=T;Dbxref=dbSNP_129:rs18271048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047407.1	dbSNP	SNV	785	785	.	+	.	ID=1368;Variant_seq=C;Dbxref=dbSNP_129:rs18271066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047407.1	dbSNP	SNV	812	812	.	+	.	ID=1369;Variant_seq=T;Dbxref=dbSNP_129:rs18271075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047407.1	dbSNP	SNV	826	826	.	+	.	ID=1370;Variant_seq=T;Dbxref=dbSNP_129:rs18271084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399003.1	dbSNP	SNV	4896	4896	.	+	.	ID=1371;Variant_seq=T;Dbxref=dbSNP_129:rs21190830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044026.1	dbSNP	SNV	89	89	.	+	.	ID=1372;Variant_seq=G;Dbxref=dbSNP_129:rs20714396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044026.1	dbSNP	SNV	3088	3088	.	+	.	ID=1373;Variant_seq=C;Dbxref=dbSNP_129:rs20715425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044026.1	dbSNP	SNV	3096	3096	.	+	.	ID=1374;Variant_seq=A;Dbxref=dbSNP_129:rs20715415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044026.1	dbSNP	SNV	3107	3107	.	+	.	ID=1375;Variant_seq=A;Dbxref=dbSNP_129:rs20715395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044026.1	dbSNP	SNV	3109	3109	.	+	.	ID=1376;Variant_seq=A;Dbxref=dbSNP_129:rs17888775;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044026.1	dbSNP	SNV	3110	3110	.	+	.	ID=1377;Variant_seq=T;Dbxref=dbSNP_129:rs20715385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044026.1	dbSNP	SNV	3122	3122	.	+	.	ID=1378;Variant_seq=A,T,G;Dbxref=dbSNP_129:rs17877580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044026.1	dbSNP	SNV	3129	3129	.	+	.	ID=1379;Variant_seq=C;Dbxref=dbSNP_129:rs20715365;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044026.1	dbSNP	SNV	3130	3130	.	+	.	ID=1380;Variant_seq=A;Dbxref=dbSNP_129:rs20715355;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044026.1	dbSNP	SNV	3131	3131	.	+	.	ID=1381;Variant_seq=A;Dbxref=dbSNP_129:rs20715345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044026.1	dbSNP	SNV	3132	3132	.	+	.	ID=1382;Variant_seq=G;Dbxref=dbSNP_129:rs20715335;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044026.1	dbSNP	SNV	3141	3141	.	+	.	ID=1383;Variant_seq=G;Dbxref=dbSNP_129:rs20715315;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044026.1	dbSNP	SNV	3152	3152	.	+	.	ID=1384;Variant_seq=A;Dbxref=dbSNP_129:rs20715305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044026.1	dbSNP	SNV	3153	3153	.	+	.	ID=1385;Variant_seq=T;Dbxref=dbSNP_129:rs20715295;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044026.1	dbSNP	SNV	3157	3157	.	+	.	ID=1386;Variant_seq=A;Dbxref=dbSNP_129:rs20715285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044026.1	dbSNP	deletion	3209	3211	.	+	.	ID=1387;Variant_seq=-;Dbxref=dbSNP_129:rs54028337;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AAA
AAAA02044026.1	dbSNP	SNV	3223	3223	.	+	.	ID=1388;Variant_seq=G;Dbxref=dbSNP_129:rs53650990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398863.1	dbSNP	SNV	719	719	.	+	.	ID=1389;Variant_seq=G;Dbxref=dbSNP_129:rs53004104;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398863.1	dbSNP	SNV	720	720	.	+	.	ID=1390;Variant_seq=T;Dbxref=dbSNP_129:rs54013410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	869	869	.	+	.	ID=1391;Variant_seq=A;Dbxref=dbSNP_129:rs53286121;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398863.1	dbSNP	SNV	870	870	.	+	.	ID=1392;Variant_seq=G;Dbxref=dbSNP_129:rs54293898;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	1901	1901	.	+	.	ID=1393;Variant_seq=C;Dbxref=dbSNP_129:rs18508731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398863.1	dbSNP	SNV	1901	1901	.	+	.	ID=1394;Variant_seq=G;Dbxref=dbSNP_129:rs21506943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398863.1	dbSNP	SNV	3887	3887	.	+	.	ID=1395;Variant_seq=T;Dbxref=dbSNP_129:rs53026363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	3912	3912	.	+	.	ID=1396;Variant_seq=T;Dbxref=dbSNP_129:rs54345502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	3925	3925	.	+	.	ID=1397;Variant_seq=T;Dbxref=dbSNP_129:rs54314325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	3931	3931	.	+	.	ID=1398;Variant_seq=C;Dbxref=dbSNP_129:rs54037207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398863.1	dbSNP	SNV	3954	3954	.	+	.	ID=1399;Variant_seq=T;Dbxref=dbSNP_129:rs53193779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	3973	3973	.	+	.	ID=1400;Variant_seq=A;Dbxref=dbSNP_129:rs53364046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398863.1	dbSNP	SNV	3983	3983	.	+	.	ID=1401;Variant_seq=T;Dbxref=dbSNP_129:rs53661978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398863.1	dbSNP	SNV	4002	4002	.	+	.	ID=1402;Variant_seq=C;Dbxref=dbSNP_129:rs53426179;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398863.1	dbSNP	SNV	6716	6716	.	+	.	ID=1403;Variant_seq=A;Dbxref=dbSNP_129:rs54014004;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038773.1	dbSNP	SNV	1511	1511	.	+	.	ID=1404;Variant_seq=T;Dbxref=dbSNP_129:rs53883170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038773.1	dbSNP	SNV	3834	3834	.	+	.	ID=1405;Variant_seq=A;Dbxref=dbSNP_129:rs54113160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038773.1	dbSNP	SNV	4981	4981	.	+	.	ID=1406;Variant_seq=C;Dbxref=dbSNP_129:rs19285142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038773.1	dbSNP	SNV	6203	6203	.	+	.	ID=1407;Variant_seq=G;Dbxref=dbSNP_129:rs18866112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038773.1	dbSNP	SNV	6904	6904	.	+	.	ID=1408;Variant_seq=T;Dbxref=dbSNP_129:rs20897706;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038773.1	dbSNP	SNV	6911	6911	.	+	.	ID=1409;Variant_seq=A;Dbxref=dbSNP_129:rs20897686;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038773.1	dbSNP	SNV	6913	6913	.	+	.	ID=1410;Variant_seq=T;Dbxref=dbSNP_129:rs20897676;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	29668	29668	.	+	.	ID=1411;Variant_seq=G;Dbxref=dbSNP_129:rs53436311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	29669	29669	.	+	.	ID=1412;Variant_seq=T;Dbxref=dbSNP_129:rs53122933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035705.1	dbSNP	SNV	29673	29673	.	+	.	ID=1413;Variant_seq=G;Dbxref=dbSNP_129:rs53359647;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	31860	31860	.	+	.	ID=1414;Variant_seq=C;Dbxref=dbSNP_129:rs53159774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035705.1	dbSNP	SNV	31886	31886	.	+	.	ID=1415;Variant_seq=A;Dbxref=dbSNP_129:rs54191482;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035705.1	dbSNP	SNV	31890	31890	.	+	.	ID=1416;Variant_seq=C;Dbxref=dbSNP_129:rs53495646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035705.1	dbSNP	SNV	31913	31913	.	+	.	ID=1417;Variant_seq=T;Dbxref=dbSNP_129:rs54390181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035705.1	dbSNP	SNV	33034	33034	.	+	.	ID=1418;Variant_seq=G;Dbxref=dbSNP_129:rs53645354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	33037	33037	.	+	.	ID=1419;Variant_seq=A;Dbxref=dbSNP_129:rs53561221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035705.1	dbSNP	SNV	33417	33417	.	+	.	ID=1420;Variant_seq=T;Dbxref=dbSNP_129:rs18863405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	34017	34017	.	+	.	ID=1421;Variant_seq=C;Dbxref=dbSNP_129:rs19810928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035705.1	dbSNP	SNV	35676	35676	.	+	.	ID=1422;Variant_seq=A;Dbxref=dbSNP_129:rs53538400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035705.1	dbSNP	SNV	35754	35754	.	+	.	ID=1423;Variant_seq=A;Dbxref=dbSNP_129:rs53463795;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035705.1	dbSNP	SNV	35758	35758	.	+	.	ID=1424;Variant_seq=T;Dbxref=dbSNP_129:rs53444095;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043162.1	dbSNP	SNV	3291	3291	.	+	.	ID=1425;Variant_seq=G;Dbxref=dbSNP_129:rs19580706;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043162.1	dbSNP	SNV	3295	3295	.	+	.	ID=1426;Variant_seq=A;Dbxref=dbSNP_129:rs19580716;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043162.1	dbSNP	SNV	3299	3299	.	+	.	ID=1427;Variant_seq=G;Dbxref=dbSNP_129:rs19580736;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043162.1	dbSNP	SNV	3300	3300	.	+	.	ID=1428;Variant_seq=A;Dbxref=dbSNP_129:rs19580746;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043162.1	dbSNP	SNV	3301	3301	.	+	.	ID=1429;Variant_seq=T;Dbxref=dbSNP_129:rs19580756;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043162.1	dbSNP	SNV	3310	3310	.	+	.	ID=1430;Variant_seq=A;Dbxref=dbSNP_129:rs19580766;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043162.1	dbSNP	SNV	3312	3312	.	+	.	ID=1431;Variant_seq=C;Dbxref=dbSNP_129:rs19580776;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043162.1	dbSNP	SNV	3313	3313	.	+	.	ID=1432;Variant_seq=T;Dbxref=dbSNP_129:rs19580786;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043162.1	dbSNP	SNV	3315	3315	.	+	.	ID=1433;Variant_seq=T;Dbxref=dbSNP_129:rs19580796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043162.1	dbSNP	SNV	3316	3316	.	+	.	ID=1434;Variant_seq=T;Dbxref=dbSNP_129:rs19580806;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	340	340	.	+	.	ID=1435;Variant_seq=A;Dbxref=dbSNP_129:rs53292718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	349	349	.	+	.	ID=1436;Variant_seq=G;Dbxref=dbSNP_129:rs53011402;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	354	354	.	+	.	ID=1437;Variant_seq=C;Dbxref=dbSNP_129:rs54087966;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	368	368	.	+	.	ID=1438;Variant_seq=C;Dbxref=dbSNP_129:rs53804961;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	369	369	.	+	.	ID=1439;Variant_seq=A;Dbxref=dbSNP_129:rs54173807;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042893.1	dbSNP	SNV	370	370	.	+	.	ID=1440;Variant_seq=A;Dbxref=dbSNP_129:rs53194844;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042893.1	dbSNP	SNV	383	383	.	+	.	ID=1441;Variant_seq=G;Dbxref=dbSNP_129:rs54400735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	387	387	.	+	.	ID=1442;Variant_seq=C;Dbxref=dbSNP_129:rs53654406;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	392	392	.	+	.	ID=1443;Variant_seq=G;Dbxref=dbSNP_129:rs53666074;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	401	401	.	+	.	ID=1444;Variant_seq=T;Dbxref=dbSNP_129:rs53623578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042893.1	dbSNP	SNV	402	402	.	+	.	ID=1445;Variant_seq=G;Dbxref=dbSNP_129:rs54138508;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	404	404	.	+	.	ID=1446;Variant_seq=T;Dbxref=dbSNP_129:rs53562902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042893.1	dbSNP	SNV	552	552	.	+	.	ID=1447;Variant_seq=A;Dbxref=dbSNP_129:rs54255135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042893.1	dbSNP	SNV	573	573	.	+	.	ID=1448;Variant_seq=T;Dbxref=dbSNP_129:rs53540146;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042893.1	dbSNP	SNV	576	576	.	+	.	ID=1449;Variant_seq=C;Dbxref=dbSNP_129:rs54272599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	deletion	582	582	.	+	.	ID=1450;Variant_seq=-;Dbxref=dbSNP_129:rs52985100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	583	583	.	+	.	ID=1451;Variant_seq=G;Dbxref=dbSNP_129:rs53785681;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042893.1	dbSNP	SNV	3137	3137	.	+	.	ID=1452;Variant_seq=A;Dbxref=dbSNP_129:rs53273988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042893.1	dbSNP	SNV	3260	3260	.	+	.	ID=1453;Variant_seq=C;Dbxref=dbSNP_129:rs53618998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399676.1	dbSNP	SNV	1384	1384	.	+	.	ID=1454;Variant_seq=G;Dbxref=dbSNP_129:rs21090585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399676.1	dbSNP	SNV	1409	1409	.	+	.	ID=1455;Variant_seq=A;Dbxref=dbSNP_129:rs21090535;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399676.1	dbSNP	SNV	1420	1420	.	+	.	ID=1456;Variant_seq=C;Dbxref=dbSNP_129:rs21090525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399676.1	dbSNP	SNV	1443	1443	.	+	.	ID=1457;Variant_seq=C;Dbxref=dbSNP_129:rs21090505;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399676.1	dbSNP	SNV	1457	1457	.	+	.	ID=1458;Variant_seq=T;Dbxref=dbSNP_129:rs21090475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399676.1	dbSNP	SNV	1467	1467	.	+	.	ID=1459;Variant_seq=T;Dbxref=dbSNP_129:rs21090445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399676.1	dbSNP	SNV	1505	1505	.	+	.	ID=1460;Variant_seq=A;Dbxref=dbSNP_129:rs21090405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399676.1	dbSNP	SNV	3698	3698	.	+	.	ID=1461;Variant_seq=C;Dbxref=dbSNP_129:rs20360325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399676.1	dbSNP	SNV	3708	3708	.	+	.	ID=1462;Variant_seq=A;Dbxref=dbSNP_129:rs20360315;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037566.1	dbSNP	SNV	149	149	.	+	.	ID=1463;Variant_seq=A;Dbxref=dbSNP_129:rs21428082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037566.1	dbSNP	SNV	2320	2320	.	+	.	ID=1464;Variant_seq=A;Dbxref=dbSNP_129:rs53598477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037566.1	dbSNP	SNV	3215	3215	.	+	.	ID=1465;Variant_seq=T;Dbxref=dbSNP_129:rs20878439;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037566.1	dbSNP	SNV	3339	3339	.	+	.	ID=1466;Variant_seq=A;Dbxref=dbSNP_129:rs20213789;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037566.1	dbSNP	SNV	9345	9345	.	+	.	ID=1467;Variant_seq=T;Dbxref=dbSNP_129:rs18725970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037566.1	dbSNP	SNV	9348	9348	.	+	.	ID=1468;Variant_seq=G;Dbxref=dbSNP_129:rs18725961;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037566.1	dbSNP	SNV	9355	9355	.	+	.	ID=1469;Variant_seq=T;Dbxref=dbSNP_129:rs18725952;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037566.1	dbSNP	SNV	9490	9490	.	+	.	ID=1470;Variant_seq=T;Dbxref=dbSNP_129:rs18725816;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044260.1	dbSNP	SNV	1038	1038	.	+	.	ID=1471;Variant_seq=G;Dbxref=dbSNP_129:rs53375079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044260.1	dbSNP	SNV	1082	1082	.	+	.	ID=1472;Variant_seq=G;Dbxref=dbSNP_129:rs54144424;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044260.1	dbSNP	SNV	1770	1770	.	+	.	ID=1473;Variant_seq=C;Dbxref=dbSNP_129:rs53270315;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044260.1	dbSNP	SNV	1787	1787	.	+	.	ID=1474;Variant_seq=T;Dbxref=dbSNP_129:rs53182017;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044260.1	dbSNP	SNV	1798	1798	.	+	.	ID=1475;Variant_seq=T;Dbxref=dbSNP_129:rs53792845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	819	819	.	+	.	ID=1476;Variant_seq=A;Dbxref=dbSNP_129:rs20817975;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	820	820	.	+	.	ID=1477;Variant_seq=A;Dbxref=dbSNP_129:rs20817985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	824	824	.	+	.	ID=1478;Variant_seq=T;Dbxref=dbSNP_129:rs20817995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398247.1	dbSNP	SNV	845	845	.	+	.	ID=1479;Variant_seq=G;Dbxref=dbSNP_129:rs20818005;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	893	893	.	+	.	ID=1480;Variant_seq=C;Dbxref=dbSNP_129:rs20818075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	904	904	.	+	.	ID=1481;Variant_seq=G;Dbxref=dbSNP_129:rs20818085;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	905	905	.	+	.	ID=1482;Variant_seq=A;Dbxref=dbSNP_129:rs20818095;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	908	908	.	+	.	ID=1483;Variant_seq=C;Dbxref=dbSNP_129:rs20818105;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	932	932	.	+	.	ID=1484;Variant_seq=C;Dbxref=dbSNP_129:rs20818125;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1053	1053	.	+	.	ID=1485;Variant_seq=C;Dbxref=dbSNP_129:rs20818255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1088	1088	.	+	.	ID=1486;Variant_seq=A;Dbxref=dbSNP_129:rs20818285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1089	1089	.	+	.	ID=1487;Variant_seq=T;Dbxref=dbSNP_129:rs20818295;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1114	1114	.	+	.	ID=1488;Variant_seq=C;Dbxref=dbSNP_129:rs20818305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1325	1325	.	+	.	ID=1489;Variant_seq=C;Dbxref=dbSNP_129:rs20818335;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1331	1331	.	+	.	ID=1490;Variant_seq=C;Dbxref=dbSNP_129:rs20818355;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1336	1336	.	+	.	ID=1491;Variant_seq=A;Dbxref=dbSNP_129:rs20818365;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1346	1346	.	+	.	ID=1492;Variant_seq=C;Dbxref=dbSNP_129:rs20818385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1354	1354	.	+	.	ID=1493;Variant_seq=C;Dbxref=dbSNP_129:rs20818395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1359	1359	.	+	.	ID=1494;Variant_seq=G;Dbxref=dbSNP_129:rs20818405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1361	1361	.	+	.	ID=1495;Variant_seq=A;Dbxref=dbSNP_129:rs20818415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398247.1	dbSNP	SNV	1362	1362	.	+	.	ID=1496;Variant_seq=A;Dbxref=dbSNP_129:rs20818425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398247.1	dbSNP	SNV	1364	1364	.	+	.	ID=1497;Variant_seq=A;Dbxref=dbSNP_129:rs20818435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1365	1365	.	+	.	ID=1498;Variant_seq=A;Dbxref=dbSNP_129:rs20818445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1379	1379	.	+	.	ID=1499;Variant_seq=G;Dbxref=dbSNP_129:rs20818455;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1389	1389	.	+	.	ID=1500;Variant_seq=T;Dbxref=dbSNP_129:rs20818475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1397	1397	.	+	.	ID=1501;Variant_seq=A;Dbxref=dbSNP_129:rs20818485;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1401	1401	.	+	.	ID=1502;Variant_seq=C;Dbxref=dbSNP_129:rs20818505;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1408	1408	.	+	.	ID=1503;Variant_seq=G;Dbxref=dbSNP_129:rs20818525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1414	1414	.	+	.	ID=1504;Variant_seq=T;Dbxref=dbSNP_129:rs20818545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1415	1415	.	+	.	ID=1505;Variant_seq=A;Dbxref=dbSNP_129:rs20818555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1426	1426	.	+	.	ID=1506;Variant_seq=G;Dbxref=dbSNP_129:rs20818575;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1427	1427	.	+	.	ID=1507;Variant_seq=G;Dbxref=dbSNP_129:rs20818585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1433	1433	.	+	.	ID=1508;Variant_seq=T;Dbxref=dbSNP_129:rs20818595;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1443	1443	.	+	.	ID=1509;Variant_seq=G;Dbxref=dbSNP_129:rs20818615;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1448	1448	.	+	.	ID=1510;Variant_seq=A;Dbxref=dbSNP_129:rs20818635;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1449	1449	.	+	.	ID=1511;Variant_seq=T;Dbxref=dbSNP_129:rs20818645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398247.1	dbSNP	SNV	1457	1457	.	+	.	ID=1512;Variant_seq=C;Dbxref=dbSNP_129:rs20818655;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1461	1461	.	+	.	ID=1513;Variant_seq=T;Dbxref=dbSNP_129:rs20818665;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1462	1462	.	+	.	ID=1514;Variant_seq=C;Dbxref=dbSNP_129:rs20818675;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1463	1463	.	+	.	ID=1515;Variant_seq=A;Dbxref=dbSNP_129:rs20818685;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	1469	1469	.	+	.	ID=1516;Variant_seq=G;Dbxref=dbSNP_129:rs20818695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1473	1473	.	+	.	ID=1517;Variant_seq=A;Dbxref=dbSNP_129:rs20818715;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	1490	1490	.	+	.	ID=1518;Variant_seq=T;Dbxref=dbSNP_129:rs20818745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1492	1492	.	+	.	ID=1519;Variant_seq=T;Dbxref=dbSNP_129:rs20818755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1514	1514	.	+	.	ID=1520;Variant_seq=C;Dbxref=dbSNP_129:rs20818765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	1637	1637	.	+	.	ID=1521;Variant_seq=A;Dbxref=dbSNP_129:rs20818815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	2449	2449	.	+	.	ID=1522;Variant_seq=T;Dbxref=dbSNP_129:rs20686215;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	31573	31573	.	+	.	ID=1523;Variant_seq=A;Dbxref=dbSNP_129:rs53677303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	40327	40327	.	+	.	ID=1524;Variant_seq=G;Dbxref=dbSNP_129:rs53554404;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398247.1	dbSNP	SNV	40330	40330	.	+	.	ID=1525;Variant_seq=A;Dbxref=dbSNP_129:rs53247000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398247.1	dbSNP	SNV	51856	51856	.	+	.	ID=1526;Variant_seq=C;Dbxref=dbSNP_129:rs18341738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398247.1	dbSNP	SNV	51948	51948	.	+	.	ID=1527;Variant_seq=T;Dbxref=dbSNP_129:rs18346488;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038782.1	dbSNP	SNV	3898	3898	.	+	.	ID=1528;Variant_seq=T;Dbxref=dbSNP_129:rs19103604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398383.1	dbSNP	SNV	13405	13405	.	+	.	ID=1529;Variant_seq=A;Dbxref=dbSNP_129:rs21167890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040575.1	dbSNP	SNV	2231	2231	.	+	.	ID=1530;Variant_seq=A;Dbxref=dbSNP_129:rs19985396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040575.1	dbSNP	SNV	2233	2233	.	+	.	ID=1531;Variant_seq=A,T,G;Dbxref=dbSNP_129:rs17892243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040575.1	dbSNP	SNV	2236	2236	.	+	.	ID=1532;Variant_seq=G;Dbxref=dbSNP_129:rs19985376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040575.1	dbSNP	SNV	2247	2247	.	+	.	ID=1533;Variant_seq=T;Dbxref=dbSNP_129:rs19985366;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042673.1	dbSNP	SNV	1689	1689	.	+	.	ID=1534;Variant_seq=T;Dbxref=dbSNP_129:rs19410267;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038725.1	dbSNP	SNV	3315	3315	.	+	.	ID=1535;Variant_seq=A,T;Dbxref=dbSNP_129:rs17888241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038725.1	dbSNP	SNV	3347	3347	.	+	.	ID=1536;Variant_seq=C;Dbxref=dbSNP_129:rs20666861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038725.1	dbSNP	SNV	3351	3351	.	+	.	ID=1537;Variant_seq=G;Dbxref=dbSNP_129:rs20666851;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038725.1	dbSNP	SNV	4332	4332	.	+	.	ID=1538;Variant_seq=G;Dbxref=dbSNP_129:rs18979222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044572.1	dbSNP	SNV	1487	1487	.	+	.	ID=1539;Variant_seq=A;Dbxref=dbSNP_129:rs52854649;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036941.1	dbSNP	SNV	3127	3127	.	+	.	ID=1540;Variant_seq=T;Dbxref=dbSNP_129:rs20193687;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036941.1	dbSNP	SNV	3585	3585	.	+	.	ID=1541;Variant_seq=A;Dbxref=dbSNP_129:rs18016563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036941.1	dbSNP	SNV	9680	9680	.	+	.	ID=1542;Variant_seq=G;Dbxref=dbSNP_129:rs53198393;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036941.1	dbSNP	SNV	9681	9681	.	+	.	ID=1543;Variant_seq=T;Dbxref=dbSNP_129:rs53659022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400086.1	dbSNP	insertion	1227	1227	.	+	.	ID=1544;Variant_seq=TTAGTGGGCAAGGTCCTC;Dbxref=dbSNP_129:rs53595848;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH400086.1	dbSNP	SNV	1349	1349	.	+	.	ID=1545;Variant_seq=T;Dbxref=dbSNP_129:rs54157637;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039811.1	dbSNP	SNV	298	298	.	+	.	ID=1546;Variant_seq=T;Dbxref=dbSNP_129:rs18279523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039811.1	dbSNP	SNV	305	305	.	+	.	ID=1547;Variant_seq=A;Dbxref=dbSNP_129:rs18279514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039811.1	dbSNP	SNV	308	308	.	+	.	ID=1548;Variant_seq=G;Dbxref=dbSNP_129:rs18279496;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039811.1	dbSNP	SNV	309	309	.	+	.	ID=1549;Variant_seq=G;Dbxref=dbSNP_129:rs18279487;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039811.1	dbSNP	SNV	310	310	.	+	.	ID=1550;Variant_seq=G;Dbxref=dbSNP_129:rs18279478;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039811.1	dbSNP	SNV	311	311	.	+	.	ID=1551;Variant_seq=T;Dbxref=dbSNP_129:rs18279469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039811.1	dbSNP	SNV	320	320	.	+	.	ID=1552;Variant_seq=C;Dbxref=dbSNP_129:rs18279460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039811.1	dbSNP	SNV	324	324	.	+	.	ID=1553;Variant_seq=T;Dbxref=dbSNP_129:rs18279451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039811.1	dbSNP	SNV	325	325	.	+	.	ID=1554;Variant_seq=A;Dbxref=dbSNP_129:rs18279442;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	779	779	.	+	.	ID=1555;Variant_seq=C;Dbxref=dbSNP_129:rs52974267;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048742.1	dbSNP	SNV	780	780	.	+	.	ID=1556;Variant_seq=C;Dbxref=dbSNP_129:rs53213843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	788	788	.	+	.	ID=1557;Variant_seq=T;Dbxref=dbSNP_129:rs53304136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048742.1	dbSNP	SNV	801	801	.	+	.	ID=1558;Variant_seq=G;Dbxref=dbSNP_129:rs53091363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048742.1	dbSNP	SNV	876	876	.	+	.	ID=1559;Variant_seq=T;Dbxref=dbSNP_129:rs20863419;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048742.1	dbSNP	SNV	892	892	.	+	.	ID=1560;Variant_seq=A;Dbxref=dbSNP_129:rs20863429;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048742.1	dbSNP	SNV	901	901	.	+	.	ID=1561;Variant_seq=C;Dbxref=dbSNP_129:rs53945283;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	903	903	.	+	.	ID=1562;Variant_seq=T;Dbxref=dbSNP_129:rs53124193;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048742.1	dbSNP	SNV	1163	1163	.	+	.	ID=1563;Variant_seq=C;Dbxref=dbSNP_129:rs54222006;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	1539	1539	.	+	.	ID=1564;Variant_seq=A;Dbxref=dbSNP_129:rs20864409;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	1696	1696	.	+	.	ID=1565;Variant_seq=C;Dbxref=dbSNP_129:rs19847297;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	1732	1732	.	+	.	ID=1566;Variant_seq=C;Dbxref=dbSNP_129:rs19847307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048742.1	dbSNP	SNV	1876	1876	.	+	.	ID=1567;Variant_seq=C;Dbxref=dbSNP_129:rs19847327;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048742.1	dbSNP	SNV	1909	1909	.	+	.	ID=1568;Variant_seq=G;Dbxref=dbSNP_129:rs52996704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048742.1	dbSNP	SNV	1910	1910	.	+	.	ID=1569;Variant_seq=C;Dbxref=dbSNP_129:rs54263689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048742.1	dbSNP	SNV	1911	1911	.	+	.	ID=1570;Variant_seq=T;Dbxref=dbSNP_129:rs54407514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043328.1	dbSNP	SNV	1755	1755	.	+	.	ID=1571;Variant_seq=T;Dbxref=dbSNP_129:rs54106542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043328.1	dbSNP	SNV	1757	1757	.	+	.	ID=1572;Variant_seq=C;Dbxref=dbSNP_129:rs54281606;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043328.1	dbSNP	SNV	1769	1769	.	+	.	ID=1573;Variant_seq=G;Dbxref=dbSNP_129:rs20933588;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043328.1	dbSNP	SNV	1770	1770	.	+	.	ID=1574;Variant_seq=C;Dbxref=dbSNP_129:rs20933578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043328.1	dbSNP	SNV	1772	1772	.	+	.	ID=1575;Variant_seq=T;Dbxref=dbSNP_129:rs52942314;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043328.1	dbSNP	SNV	1773	1773	.	+	.	ID=1576;Variant_seq=C;Dbxref=dbSNP_129:rs20933558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043328.1	dbSNP	SNV	2944	2944	.	+	.	ID=1577;Variant_seq=C;Dbxref=dbSNP_129:rs21146193;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	1008	1008	.	+	.	ID=1578;Variant_seq=A;Dbxref=dbSNP_129:rs17970769;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1013	1013	.	+	.	ID=1579;Variant_seq=G;Dbxref=dbSNP_129:rs17970778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1017	1017	.	+	.	ID=1580;Variant_seq=A;Dbxref=dbSNP_129:rs17970787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1019	1019	.	+	.	ID=1581;Variant_seq=T;Dbxref=dbSNP_129:rs17970796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1023	1023	.	+	.	ID=1582;Variant_seq=G;Dbxref=dbSNP_129:rs17970805;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1025	1025	.	+	.	ID=1583;Variant_seq=G;Dbxref=dbSNP_129:rs17970814;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1040	1040	.	+	.	ID=1584;Variant_seq=C;Dbxref=dbSNP_129:rs17970823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	1083	1083	.	+	.	ID=1585;Variant_seq=T;Dbxref=dbSNP_129:rs17970832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	1189	1189	.	+	.	ID=1586;Variant_seq=T;Dbxref=dbSNP_129:rs17970859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	1199	1199	.	+	.	ID=1587;Variant_seq=T;Dbxref=dbSNP_129:rs17970868;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1223	1223	.	+	.	ID=1588;Variant_seq=G;Dbxref=dbSNP_129:rs17970877;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1236	1236	.	+	.	ID=1589;Variant_seq=G;Dbxref=dbSNP_129:rs17970886;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1493	1493	.	+	.	ID=1590;Variant_seq=A;Dbxref=dbSNP_129:rs17970940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1506	1506	.	+	.	ID=1591;Variant_seq=T;Dbxref=dbSNP_129:rs17970949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	1580	1580	.	+	.	ID=1592;Variant_seq=G;Dbxref=dbSNP_129:rs17970985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1587	1587	.	+	.	ID=1593;Variant_seq=A;Dbxref=dbSNP_129:rs17970994;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1619	1619	.	+	.	ID=1594;Variant_seq=C;Dbxref=dbSNP_129:rs17971021;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	1624	1624	.	+	.	ID=1595;Variant_seq=A;Dbxref=dbSNP_129:rs17971030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	1647	1647	.	+	.	ID=1596;Variant_seq=T;Dbxref=dbSNP_129:rs17971057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	1648	1648	.	+	.	ID=1597;Variant_seq=C;Dbxref=dbSNP_129:rs17971066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	1649	1649	.	+	.	ID=1598;Variant_seq=A;Dbxref=dbSNP_129:rs17971075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1792	1792	.	+	.	ID=1599;Variant_seq=G;Dbxref=dbSNP_129:rs17971147;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	1906	1906	.	+	.	ID=1600;Variant_seq=A;Dbxref=dbSNP_129:rs17971183;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	1924	1924	.	+	.	ID=1601;Variant_seq=G;Dbxref=dbSNP_129:rs17971201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2044	2044	.	+	.	ID=1602;Variant_seq=T;Dbxref=dbSNP_129:rs17971237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	2055	2055	.	+	.	ID=1603;Variant_seq=A;Dbxref=dbSNP_129:rs17971264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	2056	2056	.	+	.	ID=1604;Variant_seq=C;Dbxref=dbSNP_129:rs17971273;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	2074	2074	.	+	.	ID=1605;Variant_seq=T;Dbxref=dbSNP_129:rs17971300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	2098	2098	.	+	.	ID=1606;Variant_seq=C;Dbxref=dbSNP_129:rs17971336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	2099	2099	.	+	.	ID=1607;Variant_seq=G;Dbxref=dbSNP_129:rs17971345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2121	2121	.	+	.	ID=1608;Variant_seq=G;Dbxref=dbSNP_129:rs17971363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2122	2122	.	+	.	ID=1609;Variant_seq=T;Dbxref=dbSNP_129:rs17971372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	2131	2131	.	+	.	ID=1610;Variant_seq=T;Dbxref=dbSNP_129:rs17971390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	2170	2170	.	+	.	ID=1611;Variant_seq=G;Dbxref=dbSNP_129:rs17971417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2401	2401	.	+	.	ID=1612;Variant_seq=A;Dbxref=dbSNP_129:rs17971678;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	2413	2413	.	+	.	ID=1613;Variant_seq=G;Dbxref=dbSNP_129:rs17971732;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2433	2433	.	+	.	ID=1614;Variant_seq=T;Dbxref=dbSNP_129:rs17971750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2436	2436	.	+	.	ID=1615;Variant_seq=G;Dbxref=dbSNP_129:rs17971759;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	2873	2873	.	+	.	ID=1616;Variant_seq=A;Dbxref=dbSNP_129:rs17971921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400172.1	dbSNP	SNV	2908	2908	.	+	.	ID=1617;Variant_seq=C;Dbxref=dbSNP_129:rs17971939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	2913	2913	.	+	.	ID=1618;Variant_seq=C;Dbxref=dbSNP_129:rs17971948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	3068	3068	.	+	.	ID=1619;Variant_seq=C;Dbxref=dbSNP_129:rs17971984;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	3080	3080	.	+	.	ID=1620;Variant_seq=T;Dbxref=dbSNP_129:rs17972002;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	3099	3099	.	+	.	ID=1621;Variant_seq=G;Dbxref=dbSNP_129:rs17972011;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400172.1	dbSNP	SNV	3298	3298	.	+	.	ID=1622;Variant_seq=T;Dbxref=dbSNP_129:rs17972119;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	3299	3299	.	+	.	ID=1623;Variant_seq=T;Dbxref=dbSNP_129:rs17972128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400172.1	dbSNP	SNV	3328	3328	.	+	.	ID=1624;Variant_seq=C;Dbxref=dbSNP_129:rs17972146;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400172.1	dbSNP	SNV	3445	3445	.	+	.	ID=1625;Variant_seq=C;Dbxref=dbSNP_129:rs17972227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039804.1	dbSNP	SNV	2533	2533	.	+	.	ID=1626;Variant_seq=A;Dbxref=dbSNP_129:rs53269418;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039804.1	dbSNP	SNV	2541	2541	.	+	.	ID=1627;Variant_seq=C;Dbxref=dbSNP_129:rs53781023;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039804.1	dbSNP	SNV	2548	2548	.	+	.	ID=1628;Variant_seq=G;Dbxref=dbSNP_129:rs53808725;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039804.1	dbSNP	SNV	2552	2552	.	+	.	ID=1629;Variant_seq=T;Dbxref=dbSNP_129:rs53281744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039804.1	dbSNP	SNV	3712	3712	.	+	.	ID=1630;Variant_seq=A;Dbxref=dbSNP_129:rs54410126;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041787.1	dbSNP	SNV	100	100	.	+	.	ID=1631;Variant_seq=T;Dbxref=dbSNP_129:rs20520980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041787.1	dbSNP	SNV	1777	1777	.	+	.	ID=1632;Variant_seq=A;Dbxref=dbSNP_129:rs20152306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041787.1	dbSNP	SNV	1813	1813	.	+	.	ID=1633;Variant_seq=A;Dbxref=dbSNP_129:rs20152396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041787.1	dbSNP	SNV	1814	1814	.	+	.	ID=1634;Variant_seq=C;Dbxref=dbSNP_129:rs19412334;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037722.1	dbSNP	SNV	1802	1802	.	+	.	ID=1635;Variant_seq=A;Dbxref=dbSNP_129:rs21172970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037722.1	dbSNP	SNV	1806	1806	.	+	.	ID=1636;Variant_seq=T;Dbxref=dbSNP_129:rs21172980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044148.1	dbSNP	SNV	343	343	.	+	.	ID=1637;Variant_seq=T;Dbxref=dbSNP_129:rs18868038;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044148.1	dbSNP	SNV	519	519	.	+	.	ID=1638;Variant_seq=T;Dbxref=dbSNP_129:rs18868048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044148.1	dbSNP	SNV	569	569	.	+	.	ID=1639;Variant_seq=A;Dbxref=dbSNP_129:rs18868058;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044148.1	dbSNP	SNV	637	637	.	+	.	ID=1640;Variant_seq=C;Dbxref=dbSNP_129:rs18868068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044148.1	dbSNP	SNV	747	747	.	+	.	ID=1641;Variant_seq=C;Dbxref=dbSNP_129:rs18868088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399648.1	dbSNP	SNV	591	591	.	+	.	ID=1642;Variant_seq=A;Dbxref=dbSNP_129:rs20571347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399648.1	dbSNP	SNV	772	772	.	+	.	ID=1643;Variant_seq=G;Dbxref=dbSNP_129:rs20571357;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399648.1	dbSNP	SNV	973	973	.	+	.	ID=1644;Variant_seq=A;Dbxref=dbSNP_129:rs20571387;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399648.1	dbSNP	SNV	1149	1149	.	+	.	ID=1645;Variant_seq=G;Dbxref=dbSNP_129:rs20571397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399648.1	dbSNP	SNV	1161	1161	.	+	.	ID=1646;Variant_seq=A;Dbxref=dbSNP_129:rs20571407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	8323	8323	.	+	.	ID=1647;Variant_seq=A;Dbxref=dbSNP_129:rs19813399;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	8648	8648	.	+	.	ID=1648;Variant_seq=C;Dbxref=dbSNP_129:rs19813551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398271.1	dbSNP	SNV	8716	8716	.	+	.	ID=1649;Variant_seq=C;Dbxref=dbSNP_129:rs19813561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398271.1	dbSNP	SNV	9633	9633	.	+	.	ID=1650;Variant_seq=A;Dbxref=dbSNP_129:rs19813960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	10769	10769	.	+	.	ID=1651;Variant_seq=G;Dbxref=dbSNP_129:rs19814250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398271.1	dbSNP	SNV	11548	11548	.	+	.	ID=1652;Variant_seq=A;Dbxref=dbSNP_129:rs19814310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	11603	11603	.	+	.	ID=1653;Variant_seq=T;Dbxref=dbSNP_129:rs19814320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398271.1	dbSNP	SNV	13484	13484	.	+	.	ID=1654;Variant_seq=A;Dbxref=dbSNP_129:rs19814880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	13557	13557	.	+	.	ID=1655;Variant_seq=T;Dbxref=dbSNP_129:rs19814890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398271.1	dbSNP	SNV	13621	13621	.	+	.	ID=1656;Variant_seq=C;Dbxref=dbSNP_129:rs19814900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398271.1	dbSNP	SNV	13680	13680	.	+	.	ID=1657;Variant_seq=G;Dbxref=dbSNP_129:rs19814910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398271.1	dbSNP	SNV	20587	20587	.	+	.	ID=1658;Variant_seq=A;Dbxref=dbSNP_129:rs53712045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	28974	28974	.	+	.	ID=1659;Variant_seq=T;Dbxref=dbSNP_129:rs53842017;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	30131	30131	.	+	.	ID=1660;Variant_seq=A;Dbxref=dbSNP_129:rs20599251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	30239	30239	.	+	.	ID=1661;Variant_seq=A;Dbxref=dbSNP_129:rs18725196;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	31068	31068	.	+	.	ID=1662;Variant_seq=A;Dbxref=dbSNP_129:rs19716834;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398271.1	dbSNP	SNV	34133	34133	.	+	.	ID=1663;Variant_seq=T;Dbxref=dbSNP_129:rs53405434;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398271.1	dbSNP	SNV	36075	36075	.	+	.	ID=1664;Variant_seq=A;Dbxref=dbSNP_129:rs53712045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399512.1	dbSNP	SNV	440	440	.	+	.	ID=1665;Variant_seq=T;Dbxref=dbSNP_129:rs53410145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399512.1	dbSNP	SNV	484	484	.	+	.	ID=1666;Variant_seq=A;Dbxref=dbSNP_129:rs54181904;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399512.1	dbSNP	SNV	515	515	.	+	.	ID=1667;Variant_seq=A;Dbxref=dbSNP_129:rs53354968;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399512.1	dbSNP	SNV	632	632	.	+	.	ID=1668;Variant_seq=A;Dbxref=dbSNP_129:rs53121280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399512.1	dbSNP	SNV	1003	1003	.	+	.	ID=1669;Variant_seq=T;Dbxref=dbSNP_129:rs19240700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399512.1	dbSNP	SNV	1022	1022	.	+	.	ID=1670;Variant_seq=G;Dbxref=dbSNP_129:rs53281092;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399512.1	dbSNP	SNV	1031	1031	.	+	.	ID=1671;Variant_seq=T;Dbxref=dbSNP_129:rs53817088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399512.1	dbSNP	SNV	1033	1033	.	+	.	ID=1672;Variant_seq=T;Dbxref=dbSNP_129:rs53742177;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399512.1	dbSNP	SNV	1104	1104	.	+	.	ID=1673;Variant_seq=A;Dbxref=dbSNP_129:rs19240650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399512.1	dbSNP	SNV	2746	2746	.	+	.	ID=1674;Variant_seq=A;Dbxref=dbSNP_129:rs21120025;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039801.1	dbSNP	SNV	1304	1304	.	+	.	ID=1675;Variant_seq=A;Dbxref=dbSNP_129:rs19200510;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048934.1	dbSNP	SNV	241	241	.	+	.	ID=1676;Variant_seq=T;Dbxref=dbSNP_129:rs19411530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041370.1	dbSNP	SNV	841	841	.	+	.	ID=1677;Variant_seq=C;Dbxref=dbSNP_129:rs21618924;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039542.1	dbSNP	SNV	1050	1050	.	+	.	ID=1678;Variant_seq=A;Dbxref=dbSNP_129:rs54324464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039542.1	dbSNP	SNV	1054	1054	.	+	.	ID=1679;Variant_seq=A;Dbxref=dbSNP_129:rs54226945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039542.1	dbSNP	SNV	1055	1055	.	+	.	ID=1680;Variant_seq=C;Dbxref=dbSNP_129:rs52890275;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039542.1	dbSNP	SNV	1159	1159	.	+	.	ID=1681;Variant_seq=C;Dbxref=dbSNP_129:rs54147051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042938.1	dbSNP	SNV	980	980	.	+	.	ID=1682;Variant_seq=G;Dbxref=dbSNP_129:rs52948129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042938.1	dbSNP	SNV	1870	1870	.	+	.	ID=1683;Variant_seq=T;Dbxref=dbSNP_129:rs18923580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	94	94	.	+	.	ID=1684;Variant_seq=G;Dbxref=dbSNP_129:rs20335963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	96	96	.	+	.	ID=1685;Variant_seq=A;Dbxref=dbSNP_129:rs20335953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	97	97	.	+	.	ID=1686;Variant_seq=A;Dbxref=dbSNP_129:rs20335943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	98	98	.	+	.	ID=1687;Variant_seq=A;Dbxref=dbSNP_129:rs20335933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	99	99	.	+	.	ID=1688;Variant_seq=A;Dbxref=dbSNP_129:rs20335923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	109	109	.	+	.	ID=1689;Variant_seq=T;Dbxref=dbSNP_129:rs20335893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	116	116	.	+	.	ID=1690;Variant_seq=A;Dbxref=dbSNP_129:rs20335863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	194	194	.	+	.	ID=1691;Variant_seq=A;Dbxref=dbSNP_129:rs20814200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	203	203	.	+	.	ID=1692;Variant_seq=G;Dbxref=dbSNP_129:rs20335573;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	209	209	.	+	.	ID=1693;Variant_seq=T;Dbxref=dbSNP_129:rs20335563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	215	215	.	+	.	ID=1694;Variant_seq=A;Dbxref=dbSNP_129:rs20335543;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	217	217	.	+	.	ID=1695;Variant_seq=G;Dbxref=dbSNP_129:rs20335533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	221	221	.	+	.	ID=1696;Variant_seq=A;Dbxref=dbSNP_129:rs20335523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	224	224	.	+	.	ID=1697;Variant_seq=C;Dbxref=dbSNP_129:rs20335513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	227	227	.	+	.	ID=1698;Variant_seq=G;Dbxref=dbSNP_129:rs20335483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	228	228	.	+	.	ID=1699;Variant_seq=G;Dbxref=dbSNP_129:rs20335473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	230	230	.	+	.	ID=1700;Variant_seq=T;Dbxref=dbSNP_129:rs20335463;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	232	232	.	+	.	ID=1701;Variant_seq=C;Dbxref=dbSNP_129:rs20335453;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	236	236	.	+	.	ID=1702;Variant_seq=G;Dbxref=dbSNP_129:rs20335443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	242	242	.	+	.	ID=1703;Variant_seq=G;Dbxref=dbSNP_129:rs20335423;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	243	243	.	+	.	ID=1704;Variant_seq=C;Dbxref=dbSNP_129:rs20335413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	248	248	.	+	.	ID=1705;Variant_seq=T;Dbxref=dbSNP_129:rs20335403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	251	251	.	+	.	ID=1706;Variant_seq=A;Dbxref=dbSNP_129:rs20335393;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	362	362	.	+	.	ID=1707;Variant_seq=C;Dbxref=dbSNP_129:rs20334863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	372	372	.	+	.	ID=1708;Variant_seq=T;Dbxref=dbSNP_129:rs20334833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	373	373	.	+	.	ID=1709;Variant_seq=G;Dbxref=dbSNP_129:rs20334823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	374	374	.	+	.	ID=1710;Variant_seq=G;Dbxref=dbSNP_129:rs20334813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	385	385	.	+	.	ID=1711;Variant_seq=T;Dbxref=dbSNP_129:rs20334803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	390	390	.	+	.	ID=1712;Variant_seq=T;Dbxref=dbSNP_129:rs20334793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	400	400	.	+	.	ID=1713;Variant_seq=T;Dbxref=dbSNP_129:rs20334763;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	401	401	.	+	.	ID=1714;Variant_seq=G;Dbxref=dbSNP_129:rs20334753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	402	402	.	+	.	ID=1715;Variant_seq=G;Dbxref=dbSNP_129:rs20334743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	404	404	.	+	.	ID=1716;Variant_seq=A;Dbxref=dbSNP_129:rs20334733;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	405	405	.	+	.	ID=1717;Variant_seq=A;Dbxref=dbSNP_129:rs20334723;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	408	408	.	+	.	ID=1718;Variant_seq=A;Dbxref=dbSNP_129:rs20334703;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	410	410	.	+	.	ID=1719;Variant_seq=G;Dbxref=dbSNP_129:rs20334693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	413	413	.	+	.	ID=1720;Variant_seq=T;Dbxref=dbSNP_129:rs20334683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	414	414	.	+	.	ID=1721;Variant_seq=A;Dbxref=dbSNP_129:rs20334673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	416	416	.	+	.	ID=1722;Variant_seq=A;Dbxref=dbSNP_129:rs20334653;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	420	420	.	+	.	ID=1723;Variant_seq=C;Dbxref=dbSNP_129:rs20334633;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	425	425	.	+	.	ID=1724;Variant_seq=C;Dbxref=dbSNP_129:rs20334623;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	428	428	.	+	.	ID=1725;Variant_seq=C;Dbxref=dbSNP_129:rs20334593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	435	435	.	+	.	ID=1726;Variant_seq=C;Dbxref=dbSNP_129:rs20334563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	436	436	.	+	.	ID=1727;Variant_seq=C;Dbxref=dbSNP_129:rs20334553;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	441	441	.	+	.	ID=1728;Variant_seq=C;Dbxref=dbSNP_129:rs20334533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	445	445	.	+	.	ID=1729;Variant_seq=A;Dbxref=dbSNP_129:rs20334513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	446	446	.	+	.	ID=1730;Variant_seq=A;Dbxref=dbSNP_129:rs20334503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	452	452	.	+	.	ID=1731;Variant_seq=T;Dbxref=dbSNP_129:rs20334473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	457	457	.	+	.	ID=1732;Variant_seq=T;Dbxref=dbSNP_129:rs20334443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	458	458	.	+	.	ID=1733;Variant_seq=C;Dbxref=dbSNP_129:rs20334433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	460	460	.	+	.	ID=1734;Variant_seq=C;Dbxref=dbSNP_129:rs20334423;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	461	461	.	+	.	ID=1735;Variant_seq=T;Dbxref=dbSNP_129:rs20334413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	465	465	.	+	.	ID=1736;Variant_seq=C;Dbxref=dbSNP_129:rs20334403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	557	557	.	+	.	ID=1737;Variant_seq=C;Dbxref=dbSNP_129:rs20334049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	565	565	.	+	.	ID=1738;Variant_seq=G;Dbxref=dbSNP_129:rs20334029;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	566	566	.	+	.	ID=1739;Variant_seq=G;Dbxref=dbSNP_129:rs20334019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	579	579	.	+	.	ID=1740;Variant_seq=C;Dbxref=dbSNP_129:rs20333999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	581	581	.	+	.	ID=1741;Variant_seq=A;Dbxref=dbSNP_129:rs20333989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400999.1	dbSNP	SNV	585	585	.	+	.	ID=1742;Variant_seq=A;Dbxref=dbSNP_129:rs20333969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	588	588	.	+	.	ID=1743;Variant_seq=A;Dbxref=dbSNP_129:rs20333949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	589	589	.	+	.	ID=1744;Variant_seq=C;Dbxref=dbSNP_129:rs20333939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	600	600	.	+	.	ID=1745;Variant_seq=T;Dbxref=dbSNP_129:rs20333919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400999.1	dbSNP	SNV	605	605	.	+	.	ID=1746;Variant_seq=G;Dbxref=dbSNP_129:rs20333909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400999.1	dbSNP	SNV	608	608	.	+	.	ID=1747;Variant_seq=G;Dbxref=dbSNP_129:rs20333899;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400999.1	dbSNP	SNV	615	615	.	+	.	ID=1748;Variant_seq=G;Dbxref=dbSNP_129:rs20333879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049308.1	dbSNP	SNV	1257	1257	.	+	.	ID=1749;Variant_seq=G;Dbxref=dbSNP_129:rs17987350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037303.1	dbSNP	SNV	10281	10281	.	+	.	ID=1750;Variant_seq=C;Dbxref=dbSNP_129:rs21623176;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037303.1	dbSNP	SNV	10282	10282	.	+	.	ID=1751;Variant_seq=G;Dbxref=dbSNP_129:rs21623185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037303.1	dbSNP	SNV	10283	10283	.	+	.	ID=1752;Variant_seq=C;Dbxref=dbSNP_129:rs21623194;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037303.1	dbSNP	SNV	10286	10286	.	+	.	ID=1753;Variant_seq=C;Dbxref=dbSNP_129:rs21623203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037303.1	dbSNP	SNV	10291	10291	.	+	.	ID=1754;Variant_seq=T;Dbxref=dbSNP_129:rs21623212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037303.1	dbSNP	SNV	10306	10306	.	+	.	ID=1755;Variant_seq=C;Dbxref=dbSNP_129:rs21623221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037303.1	dbSNP	SNV	10311	10311	.	+	.	ID=1756;Variant_seq=T;Dbxref=dbSNP_129:rs21623230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037303.1	dbSNP	SNV	10673	10673	.	+	.	ID=1757;Variant_seq=T;Dbxref=dbSNP_129:rs19094139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037303.1	dbSNP	SNV	10677	10677	.	+	.	ID=1758;Variant_seq=A;Dbxref=dbSNP_129:rs19094149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037303.1	dbSNP	SNV	10690	10690	.	+	.	ID=1759;Variant_seq=A;Dbxref=dbSNP_129:rs19094199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035694.1	dbSNP	SNV	30104	30104	.	+	.	ID=1760;Variant_seq=T;Dbxref=dbSNP_129:rs19393604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035694.1	dbSNP	SNV	32160	32160	.	+	.	ID=1761;Variant_seq=A;Dbxref=dbSNP_129:rs21645525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399254.1	dbSNP	SNV	4175	4175	.	+	.	ID=1762;Variant_seq=T;Dbxref=dbSNP_129:rs18153812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399254.1	dbSNP	SNV	4202	4202	.	+	.	ID=1763;Variant_seq=G;Dbxref=dbSNP_129:rs18153830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399254.1	dbSNP	SNV	5488	5488	.	+	.	ID=1764;Variant_seq=C;Dbxref=dbSNP_129:rs18155252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045263.1	dbSNP	SNV	2740	2740	.	+	.	ID=1765;Variant_seq=T;Dbxref=dbSNP_129:rs21612853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037768.1	dbSNP	SNV	285	285	.	+	.	ID=1766;Variant_seq=A;Dbxref=dbSNP_129:rs53010757;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037768.1	dbSNP	SNV	287	287	.	+	.	ID=1767;Variant_seq=G;Dbxref=dbSNP_129:rs53965848;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037768.1	dbSNP	SNV	294	294	.	+	.	ID=1768;Variant_seq=T;Dbxref=dbSNP_129:rs53567756;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037768.1	dbSNP	SNV	299	299	.	+	.	ID=1769;Variant_seq=T;Dbxref=dbSNP_129:rs53043192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037768.1	dbSNP	SNV	303	303	.	+	.	ID=1770;Variant_seq=T;Dbxref=dbSNP_129:rs53475509;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037768.1	dbSNP	SNV	2057	2057	.	+	.	ID=1771;Variant_seq=T;Dbxref=dbSNP_129:rs20818142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037768.1	dbSNP	SNV	4305	4305	.	+	.	ID=1772;Variant_seq=T;Dbxref=dbSNP_129:rs19077457;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037768.1	dbSNP	SNV	4745	4745	.	+	.	ID=1773;Variant_seq=A;Dbxref=dbSNP_129:rs18973839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046969.1	dbSNP	SNV	878	878	.	+	.	ID=1774;Variant_seq=G;Dbxref=dbSNP_129:rs21077519;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399594.1	dbSNP	SNV	2593	2593	.	+	.	ID=1775;Variant_seq=A;Dbxref=dbSNP_129:rs21519788;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399594.1	dbSNP	SNV	2774	2774	.	+	.	ID=1776;Variant_seq=A;Dbxref=dbSNP_129:rs19007919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399594.1	dbSNP	SNV	4422	4422	.	+	.	ID=1777;Variant_seq=A;Dbxref=dbSNP_129:rs52862181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399594.1	dbSNP	SNV	4427	4427	.	+	.	ID=1778;Variant_seq=T;Dbxref=dbSNP_129:rs53305210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399306.1	dbSNP	SNV	611	611	.	+	.	ID=1779;Variant_seq=A;Dbxref=dbSNP_129:rs20888499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399306.1	dbSNP	SNV	1245	1245	.	+	.	ID=1780;Variant_seq=G;Dbxref=dbSNP_129:rs19999614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399306.1	dbSNP	SNV	1246	1246	.	+	.	ID=1781;Variant_seq=A;Dbxref=dbSNP_129:rs19999635;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399306.1	dbSNP	SNV	1249	1249	.	+	.	ID=1782;Variant_seq=G;Dbxref=dbSNP_129:rs19999681;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399306.1	dbSNP	SNV	1250	1250	.	+	.	ID=1783;Variant_seq=T;Dbxref=dbSNP_129:rs19999706;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399306.1	dbSNP	SNV	2196	2196	.	+	.	ID=1784;Variant_seq=A;Dbxref=dbSNP_129:rs18913414;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399306.1	dbSNP	SNV	2223	2223	.	+	.	ID=1785;Variant_seq=A;Dbxref=dbSNP_129:rs19499269;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399306.1	dbSNP	SNV	3305	3305	.	+	.	ID=1786;Variant_seq=A;Dbxref=dbSNP_129:rs20463806;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399306.1	dbSNP	SNV	3309	3309	.	+	.	ID=1787;Variant_seq=C;Dbxref=dbSNP_129:rs20463786;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399306.1	dbSNP	SNV	3311	3311	.	+	.	ID=1788;Variant_seq=T;Dbxref=dbSNP_129:rs20463776;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	1596	1596	.	+	.	ID=1789;Variant_seq=T;Dbxref=dbSNP_129:rs20469831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12244	12244	.	+	.	ID=1790;Variant_seq=G;Dbxref=dbSNP_129:rs21765973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	12381	12381	.	+	.	ID=1791;Variant_seq=C;Dbxref=dbSNP_129:rs21765991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12406	12406	.	+	.	ID=1792;Variant_seq=G;Dbxref=dbSNP_129:rs21766000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	12409	12409	.	+	.	ID=1793;Variant_seq=T;Dbxref=dbSNP_129:rs21766009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	12442	12442	.	+	.	ID=1794;Variant_seq=C;Dbxref=dbSNP_129:rs21766027;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12453	12453	.	+	.	ID=1795;Variant_seq=C;Dbxref=dbSNP_129:rs21766045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12515	12515	.	+	.	ID=1796;Variant_seq=G;Dbxref=dbSNP_129:rs21766063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12551	12551	.	+	.	ID=1797;Variant_seq=C;Dbxref=dbSNP_129:rs21766081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12636	12636	.	+	.	ID=1798;Variant_seq=A;Dbxref=dbSNP_129:rs21766099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12641	12641	.	+	.	ID=1799;Variant_seq=T;Dbxref=dbSNP_129:rs21766108;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	12737	12737	.	+	.	ID=1800;Variant_seq=A;Dbxref=dbSNP_129:rs21766180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12773	12773	.	+	.	ID=1801;Variant_seq=T;Dbxref=dbSNP_129:rs21766198;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12777	12777	.	+	.	ID=1802;Variant_seq=T;Dbxref=dbSNP_129:rs21766207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	12791	12791	.	+	.	ID=1803;Variant_seq=C;Dbxref=dbSNP_129:rs21766216;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12793	12793	.	+	.	ID=1804;Variant_seq=A;Dbxref=dbSNP_129:rs21766225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12813	12813	.	+	.	ID=1805;Variant_seq=C;Dbxref=dbSNP_129:rs21766243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12816	12816	.	+	.	ID=1806;Variant_seq=A;Dbxref=dbSNP_129:rs21766252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12825	12825	.	+	.	ID=1807;Variant_seq=A;Dbxref=dbSNP_129:rs21766270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12900	12900	.	+	.	ID=1808;Variant_seq=C;Dbxref=dbSNP_129:rs21766279;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12935	12935	.	+	.	ID=1809;Variant_seq=C;Dbxref=dbSNP_129:rs21766297;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	12941	12941	.	+	.	ID=1810;Variant_seq=A;Dbxref=dbSNP_129:rs21766306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12944	12944	.	+	.	ID=1811;Variant_seq=G;Dbxref=dbSNP_129:rs21766315;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	12948	12948	.	+	.	ID=1812;Variant_seq=C;Dbxref=dbSNP_129:rs21766324;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12949	12949	.	+	.	ID=1813;Variant_seq=T;Dbxref=dbSNP_129:rs21766333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	12984	12984	.	+	.	ID=1814;Variant_seq=C;Dbxref=dbSNP_129:rs21766342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13015	13015	.	+	.	ID=1815;Variant_seq=T;Dbxref=dbSNP_129:rs20710431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13020	13020	.	+	.	ID=1816;Variant_seq=G;Dbxref=dbSNP_129:rs21766360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13056	13056	.	+	.	ID=1817;Variant_seq=T;Dbxref=dbSNP_129:rs21766369;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13091	13091	.	+	.	ID=1818;Variant_seq=A;Dbxref=dbSNP_129:rs21766405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13116	13116	.	+	.	ID=1819;Variant_seq=G;Dbxref=dbSNP_129:rs21766432;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13131	13131	.	+	.	ID=1820;Variant_seq=G;Dbxref=dbSNP_129:rs21766468;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13167	13167	.	+	.	ID=1821;Variant_seq=T;Dbxref=dbSNP_129:rs21766486;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13172	13172	.	+	.	ID=1822;Variant_seq=T;Dbxref=dbSNP_129:rs21766495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13176	13176	.	+	.	ID=1823;Variant_seq=C;Dbxref=dbSNP_129:rs21766504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13181	13181	.	+	.	ID=1824;Variant_seq=T;Dbxref=dbSNP_129:rs21766522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13187	13187	.	+	.	ID=1825;Variant_seq=G;Dbxref=dbSNP_129:rs21766531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13188	13188	.	+	.	ID=1826;Variant_seq=C;Dbxref=dbSNP_129:rs21766540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13196	13196	.	+	.	ID=1827;Variant_seq=A;Dbxref=dbSNP_129:rs21766558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	13281	13281	.	+	.	ID=1828;Variant_seq=A;Dbxref=dbSNP_129:rs21766639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	13521	13521	.	+	.	ID=1829;Variant_seq=T;Dbxref=dbSNP_129:rs21766747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13754	13754	.	+	.	ID=1830;Variant_seq=A;Dbxref=dbSNP_129:rs21766818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	13763	13763	.	+	.	ID=1831;Variant_seq=G;Dbxref=dbSNP_129:rs21766827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	13767	13767	.	+	.	ID=1832;Variant_seq=A;Dbxref=dbSNP_129:rs21766836;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	13781	13781	.	+	.	ID=1833;Variant_seq=T;Dbxref=dbSNP_129:rs21766845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13784	13784	.	+	.	ID=1834;Variant_seq=C;Dbxref=dbSNP_129:rs21766854;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13795	13795	.	+	.	ID=1835;Variant_seq=T;Dbxref=dbSNP_129:rs21766863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398376.1	dbSNP	SNV	13814	13814	.	+	.	ID=1836;Variant_seq=C;Dbxref=dbSNP_129:rs21766872;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13946	13946	.	+	.	ID=1837;Variant_seq=C;Dbxref=dbSNP_129:rs21766899;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	13959	13959	.	+	.	ID=1838;Variant_seq=G;Dbxref=dbSNP_129:rs21766907;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398376.1	dbSNP	SNV	15844	15844	.	+	.	ID=1839;Variant_seq=A;Dbxref=dbSNP_129:rs21696646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398376.1	dbSNP	SNV	17810	17810	.	+	.	ID=1840;Variant_seq=C;Dbxref=dbSNP_129:rs18683717;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398376.1	dbSNP	SNV	18517	18517	.	+	.	ID=1841;Variant_seq=A;Dbxref=dbSNP_129:rs21383721;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399457.1	dbSNP	SNV	77	77	.	+	.	ID=1842;Variant_seq=A;Dbxref=dbSNP_129:rs19539481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399457.1	dbSNP	SNV	818	818	.	+	.	ID=1843;Variant_seq=G;Dbxref=dbSNP_129:rs21782784;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399457.1	dbSNP	SNV	2104	2104	.	+	.	ID=1844;Variant_seq=A;Dbxref=dbSNP_129:rs20918489;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399457.1	dbSNP	SNV	2200	2200	.	+	.	ID=1845;Variant_seq=T;Dbxref=dbSNP_129:rs20918459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398507.1	dbSNP	SNV	5728	5728	.	+	.	ID=1846;Variant_seq=T;Dbxref=dbSNP_129:rs18107384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398507.1	dbSNP	SNV	6766	6766	.	+	.	ID=1847;Variant_seq=G;Dbxref=dbSNP_129:rs19281549;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398507.1	dbSNP	SNV	10911	10911	.	+	.	ID=1848;Variant_seq=A;Dbxref=dbSNP_129:rs53333530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036946.1	dbSNP	SNV	1508	1508	.	+	.	ID=1849;Variant_seq=T;Dbxref=dbSNP_129:rs21543347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036946.1	dbSNP	SNV	1687	1687	.	+	.	ID=1850;Variant_seq=T;Dbxref=dbSNP_129:rs18865591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036946.1	dbSNP	SNV	3458	3458	.	+	.	ID=1851;Variant_seq=G;Dbxref=dbSNP_129:rs53791318;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399980.1	dbSNP	SNV	294	294	.	+	.	ID=1852;Variant_seq=A;Dbxref=dbSNP_129:rs54339963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399980.1	dbSNP	SNV	382	382	.	+	.	ID=1853;Variant_seq=T;Dbxref=dbSNP_129:rs53583745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399980.1	dbSNP	SNV	2786	2786	.	+	.	ID=1854;Variant_seq=A;Dbxref=dbSNP_129:rs53358922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399980.1	dbSNP	SNV	2789	2789	.	+	.	ID=1855;Variant_seq=T;Dbxref=dbSNP_129:rs53190351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399980.1	dbSNP	SNV	2790	2790	.	+	.	ID=1856;Variant_seq=T;Dbxref=dbSNP_129:rs52964926;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399980.1	dbSNP	SNV	2793	2793	.	+	.	ID=1857;Variant_seq=A;Dbxref=dbSNP_129:rs52980514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399980.1	dbSNP	SNV	2853	2853	.	+	.	ID=1858;Variant_seq=A;Dbxref=dbSNP_129:rs53647663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399980.1	dbSNP	SNV	2874	2874	.	+	.	ID=1859;Variant_seq=T;Dbxref=dbSNP_129:rs53129245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399980.1	dbSNP	SNV	3061	3061	.	+	.	ID=1860;Variant_seq=A;Dbxref=dbSNP_129:rs54324385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037562.1	dbSNP	SNV	6185	6185	.	+	.	ID=1861;Variant_seq=T;Dbxref=dbSNP_129:rs21528032;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037562.1	dbSNP	SNV	6191	6191	.	+	.	ID=1862;Variant_seq=C;Dbxref=dbSNP_129:rs21528052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037562.1	dbSNP	SNV	6193	6193	.	+	.	ID=1863;Variant_seq=T;Dbxref=dbSNP_129:rs21528062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037562.1	dbSNP	SNV	6201	6201	.	+	.	ID=1864;Variant_seq=T;Dbxref=dbSNP_129:rs21528072;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401010.1	dbSNP	SNV	240	240	.	+	.	ID=1865;Variant_seq=T;Dbxref=dbSNP_129:rs19560133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401010.1	dbSNP	SNV	555	555	.	+	.	ID=1866;Variant_seq=A;Dbxref=dbSNP_129:rs53307729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401010.1	dbSNP	SNV	707	707	.	+	.	ID=1867;Variant_seq=T;Dbxref=dbSNP_129:rs53756282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401010.1	dbSNP	SNV	827	827	.	+	.	ID=1868;Variant_seq=A;Dbxref=dbSNP_129:rs53665607;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050008.1	dbSNP	SNV	508	508	.	+	.	ID=1869;Variant_seq=G;Dbxref=dbSNP_129:rs21501407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398941.1	dbSNP	SNV	541	541	.	+	.	ID=1870;Variant_seq=T;Dbxref=dbSNP_129:rs52955354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398941.1	dbSNP	SNV	3486	3486	.	+	.	ID=1871;Variant_seq=A;Dbxref=dbSNP_129:rs53996622;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398941.1	dbSNP	SNV	3501	3501	.	+	.	ID=1872;Variant_seq=C;Dbxref=dbSNP_129:rs53534534;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398941.1	dbSNP	SNV	3508	3508	.	+	.	ID=1873;Variant_seq=T;Dbxref=dbSNP_129:rs53982662;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398941.1	dbSNP	SNV	5018	5018	.	+	.	ID=1874;Variant_seq=G;Dbxref=dbSNP_129:rs20692936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398941.1	dbSNP	SNV	7672	7672	.	+	.	ID=1875;Variant_seq=A;Dbxref=dbSNP_129:rs53641615;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044341.1	dbSNP	SNV	355	355	.	+	.	ID=1876;Variant_seq=C;Dbxref=dbSNP_129:rs53413589;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044341.1	dbSNP	SNV	391	391	.	+	.	ID=1877;Variant_seq=C;Dbxref=dbSNP_129:rs54283245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044341.1	dbSNP	SNV	1937	1937	.	+	.	ID=1878;Variant_seq=A;Dbxref=dbSNP_129:rs20771860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044341.1	dbSNP	SNV	1937	1937	.	+	.	ID=1879;Variant_seq=A;Dbxref=dbSNP_129:rs52968487;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044341.1	dbSNP	SNV	1995	1995	.	+	.	ID=1880;Variant_seq=C;Dbxref=dbSNP_129:rs52990477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044341.1	dbSNP	SNV	2867	2867	.	+	.	ID=1881;Variant_seq=C;Dbxref=dbSNP_129:rs20771950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044341.1	dbSNP	SNV	2958	2958	.	+	.	ID=1882;Variant_seq=T;Dbxref=dbSNP_129:rs20771960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044341.1	dbSNP	SNV	3152	3152	.	+	.	ID=1883;Variant_seq=T;Dbxref=dbSNP_129:rs20771970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041657.1	dbSNP	SNV	1578	1578	.	+	.	ID=1884;Variant_seq=A;Dbxref=dbSNP_129:rs54096994;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	1978	1978	.	+	.	ID=1885;Variant_seq=A;Dbxref=dbSNP_129:rs20947354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	2594	2594	.	+	.	ID=1886;Variant_seq=G;Dbxref=dbSNP_129:rs18670992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041657.1	dbSNP	SNV	2801	2801	.	+	.	ID=1887;Variant_seq=T;Dbxref=dbSNP_129:rs18670965;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	2868	2868	.	+	.	ID=1888;Variant_seq=G;Dbxref=dbSNP_129:rs18670947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	2959	2959	.	+	.	ID=1889;Variant_seq=T;Dbxref=dbSNP_129:rs18670938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	3116	3116	.	+	.	ID=1890;Variant_seq=G;Dbxref=dbSNP_129:rs18670911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	3164	3164	.	+	.	ID=1891;Variant_seq=C;Dbxref=dbSNP_129:rs18670902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041657.1	dbSNP	SNV	3448	3448	.	+	.	ID=1892;Variant_seq=T;Dbxref=dbSNP_129:rs18670857;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	3473	3473	.	+	.	ID=1893;Variant_seq=A;Dbxref=dbSNP_129:rs18670848;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041657.1	dbSNP	SNV	3528	3528	.	+	.	ID=1894;Variant_seq=A;Dbxref=dbSNP_129:rs18670830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041657.1	dbSNP	SNV	3626	3626	.	+	.	ID=1895;Variant_seq=G;Dbxref=dbSNP_129:rs18670812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	3840	3840	.	+	.	ID=1896;Variant_seq=A;Dbxref=dbSNP_129:rs18670785;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041657.1	dbSNP	SNV	3841	3841	.	+	.	ID=1897;Variant_seq=C;Dbxref=dbSNP_129:rs18670776;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041657.1	dbSNP	SNV	3862	3862	.	+	.	ID=1898;Variant_seq=G;Dbxref=dbSNP_129:rs18670767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	3911	3911	.	+	.	ID=1899;Variant_seq=A;Dbxref=dbSNP_129:rs18670758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041657.1	dbSNP	SNV	3926	3926	.	+	.	ID=1900;Variant_seq=G;Dbxref=dbSNP_129:rs18670749;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	4152	4152	.	+	.	ID=1901;Variant_seq=G;Dbxref=dbSNP_129:rs18670704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	4165	4165	.	+	.	ID=1902;Variant_seq=T;Dbxref=dbSNP_129:rs18670695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	4166	4166	.	+	.	ID=1903;Variant_seq=T;Dbxref=dbSNP_129:rs18670686;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041657.1	dbSNP	SNV	4330	4330	.	+	.	ID=1904;Variant_seq=C;Dbxref=dbSNP_129:rs18670668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041657.1	dbSNP	SNV	4337	4337	.	+	.	ID=1905;Variant_seq=G;Dbxref=dbSNP_129:rs18670659;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	4367	4367	.	+	.	ID=1906;Variant_seq=G;Dbxref=dbSNP_129:rs18670650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041657.1	dbSNP	SNV	4395	4395	.	+	.	ID=1907;Variant_seq=G;Dbxref=dbSNP_129:rs18670641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047517.1	dbSNP	SNV	1020	1020	.	+	.	ID=1908;Variant_seq=T;Dbxref=dbSNP_129:rs20279168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400217.1	dbSNP	SNV	2775	2775	.	+	.	ID=1909;Variant_seq=G;Dbxref=dbSNP_129:rs19973476;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042369.1	dbSNP	SNV	2116	2116	.	+	.	ID=1910;Variant_seq=A;Dbxref=dbSNP_129:rs20546317;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042369.1	dbSNP	SNV	2143	2143	.	+	.	ID=1911;Variant_seq=T;Dbxref=dbSNP_129:rs20546267;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042369.1	dbSNP	SNV	2270	2270	.	+	.	ID=1912;Variant_seq=A;Dbxref=dbSNP_129:rs20306232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	165	165	.	+	.	ID=1913;Variant_seq=T;Dbxref=dbSNP_129:rs19700003;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	241	241	.	+	.	ID=1914;Variant_seq=C;Dbxref=dbSNP_129:rs19700013;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039304.1	dbSNP	SNV	257	257	.	+	.	ID=1915;Variant_seq=A;Dbxref=dbSNP_129:rs19700023;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	395	395	.	+	.	ID=1916;Variant_seq=A;Dbxref=dbSNP_129:rs19700043;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	405	405	.	+	.	ID=1917;Variant_seq=T;Dbxref=dbSNP_129:rs19700053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	430	430	.	+	.	ID=1918;Variant_seq=A;Dbxref=dbSNP_129:rs19700063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	497	497	.	+	.	ID=1919;Variant_seq=G;Dbxref=dbSNP_129:rs19700073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039304.1	dbSNP	SNV	514	514	.	+	.	ID=1920;Variant_seq=C;Dbxref=dbSNP_129:rs19700093;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039304.1	dbSNP	SNV	533	533	.	+	.	ID=1921;Variant_seq=C;Dbxref=dbSNP_129:rs19700103;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039304.1	dbSNP	SNV	769	769	.	+	.	ID=1922;Variant_seq=T;Dbxref=dbSNP_129:rs19700163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	777	777	.	+	.	ID=1923;Variant_seq=A;Dbxref=dbSNP_129:rs19700173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	1751	1751	.	+	.	ID=1924;Variant_seq=A;Dbxref=dbSNP_129:rs20647325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	3318	3318	.	+	.	ID=1925;Variant_seq=A;Dbxref=dbSNP_129:rs54266597;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	3322	3322	.	+	.	ID=1926;Variant_seq=A,T;Dbxref=dbSNP_129:rs53047621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	3324	3324	.	+	.	ID=1927;Variant_seq=A;Dbxref=dbSNP_129:rs53550397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	3327	3327	.	+	.	ID=1928;Variant_seq=T;Dbxref=dbSNP_129:rs53169376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	4160	4160	.	+	.	ID=1929;Variant_seq=A;Dbxref=dbSNP_129:rs19287656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	4225	4225	.	+	.	ID=1930;Variant_seq=T;Dbxref=dbSNP_129:rs54035870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	4226	4226	.	+	.	ID=1931;Variant_seq=A;Dbxref=dbSNP_129:rs54112513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	4232	4232	.	+	.	ID=1932;Variant_seq=A;Dbxref=dbSNP_129:rs52927465;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	4236	4236	.	+	.	ID=1933;Variant_seq=A;Dbxref=dbSNP_129:rs52870750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	4237	4237	.	+	.	ID=1934;Variant_seq=T;Dbxref=dbSNP_129:rs53248399;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	4246	4246	.	+	.	ID=1935;Variant_seq=A;Dbxref=dbSNP_129:rs53108783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039304.1	dbSNP	SNV	4253	4253	.	+	.	ID=1936;Variant_seq=T;Dbxref=dbSNP_129:rs53992483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039304.1	dbSNP	SNV	4254	4254	.	+	.	ID=1937;Variant_seq=A;Dbxref=dbSNP_129:rs53017461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	4257	4257	.	+	.	ID=1938;Variant_seq=A;Dbxref=dbSNP_129:rs53602141;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039304.1	dbSNP	SNV	4260	4260	.	+	.	ID=1939;Variant_seq=T;Dbxref=dbSNP_129:rs54352104;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039304.1	dbSNP	SNV	6206	6206	.	+	.	ID=1940;Variant_seq=C;Dbxref=dbSNP_129:rs53744250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	160	160	.	+	.	ID=1941;Variant_seq=A;Dbxref=dbSNP_129:rs54274187;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	562	562	.	+	.	ID=1942;Variant_seq=C;Dbxref=dbSNP_129:rs20893909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	565	565	.	+	.	ID=1943;Variant_seq=C;Dbxref=dbSNP_129:rs20893919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	568	568	.	+	.	ID=1944;Variant_seq=A;Dbxref=dbSNP_129:rs20893929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	574	574	.	+	.	ID=1945;Variant_seq=G;Dbxref=dbSNP_129:rs20893939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	577	577	.	+	.	ID=1946;Variant_seq=T;Dbxref=dbSNP_129:rs20893959;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	578	578	.	+	.	ID=1947;Variant_seq=A;Dbxref=dbSNP_129:rs20893969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	610	610	.	+	.	ID=1948;Variant_seq=T;Dbxref=dbSNP_129:rs20894019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	613	613	.	+	.	ID=1949;Variant_seq=C;Dbxref=dbSNP_129:rs20894029;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	616	616	.	+	.	ID=1950;Variant_seq=T;Dbxref=dbSNP_129:rs20894039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	620	620	.	+	.	ID=1951;Variant_seq=C;Dbxref=dbSNP_129:rs20894049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	622	622	.	+	.	ID=1952;Variant_seq=T;Dbxref=dbSNP_129:rs20894059;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	625	625	.	+	.	ID=1953;Variant_seq=G;Dbxref=dbSNP_129:rs20894069;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	634	634	.	+	.	ID=1954;Variant_seq=C;Dbxref=dbSNP_129:rs20894089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	637	637	.	+	.	ID=1955;Variant_seq=C;Dbxref=dbSNP_129:rs20894099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	652	652	.	+	.	ID=1956;Variant_seq=C;Dbxref=dbSNP_129:rs20894109;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	814	814	.	+	.	ID=1957;Variant_seq=A;Dbxref=dbSNP_129:rs20894478;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	817	817	.	+	.	ID=1958;Variant_seq=G;Dbxref=dbSNP_129:rs20894488;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	820	820	.	+	.	ID=1959;Variant_seq=A,C;Dbxref=dbSNP_129:rs17877157;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	826	826	.	+	.	ID=1960;Variant_seq=C;Dbxref=dbSNP_129:rs20894508;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	827	827	.	+	.	ID=1961;Variant_seq=A;Dbxref=dbSNP_129:rs20894518;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	829	829	.	+	.	ID=1962;Variant_seq=C;Dbxref=dbSNP_129:rs20894528;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	841	841	.	+	.	ID=1963;Variant_seq=G;Dbxref=dbSNP_129:rs20894548;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	850	850	.	+	.	ID=1964;Variant_seq=G;Dbxref=dbSNP_129:rs20894558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	854	854	.	+	.	ID=1965;Variant_seq=A;Dbxref=dbSNP_129:rs20894568;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	860	860	.	+	.	ID=1966;Variant_seq=A;Dbxref=dbSNP_129:rs20894588;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	862	862	.	+	.	ID=1967;Variant_seq=T;Dbxref=dbSNP_129:rs20894598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	865	865	.	+	.	ID=1968;Variant_seq=T;Dbxref=dbSNP_129:rs20894618;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	869	869	.	+	.	ID=1969;Variant_seq=C;Dbxref=dbSNP_129:rs20894628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	874	874	.	+	.	ID=1970;Variant_seq=G;Dbxref=dbSNP_129:rs20894648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	877	877	.	+	.	ID=1971;Variant_seq=C;Dbxref=dbSNP_129:rs20894678;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	880	880	.	+	.	ID=1972;Variant_seq=T;Dbxref=dbSNP_129:rs20894688;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	886	886	.	+	.	ID=1973;Variant_seq=A;Dbxref=dbSNP_129:rs20894698;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	889	889	.	+	.	ID=1974;Variant_seq=G;Dbxref=dbSNP_129:rs20894718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400516.1	dbSNP	SNV	898	898	.	+	.	ID=1975;Variant_seq=C;Dbxref=dbSNP_129:rs20894728;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	899	899	.	+	.	ID=1976;Variant_seq=A;Dbxref=dbSNP_129:rs20894738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	901	901	.	+	.	ID=1977;Variant_seq=G;Dbxref=dbSNP_129:rs20894758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400516.1	dbSNP	SNV	902	902	.	+	.	ID=1978;Variant_seq=A;Dbxref=dbSNP_129:rs20894768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400516.1	dbSNP	SNV	904	904	.	+	.	ID=1979;Variant_seq=G;Dbxref=dbSNP_129:rs20894778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400516.1	dbSNP	SNV	908	908	.	+	.	ID=1980;Variant_seq=A;Dbxref=dbSNP_129:rs20894798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399821.1	dbSNP	SNV	716	716	.	+	.	ID=1981;Variant_seq=C;Dbxref=dbSNP_129:rs20259494;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399821.1	dbSNP	SNV	740	740	.	+	.	ID=1982;Variant_seq=G;Dbxref=dbSNP_129:rs20259422;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399821.1	dbSNP	SNV	800	800	.	+	.	ID=1983;Variant_seq=A;Dbxref=dbSNP_129:rs20259172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399821.1	dbSNP	SNV	812	812	.	+	.	ID=1984;Variant_seq=T;Dbxref=dbSNP_129:rs20259102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399038.1	dbSNP	SNV	832	832	.	+	.	ID=1985;Variant_seq=G;Dbxref=dbSNP_129:rs20745041;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399038.1	dbSNP	SNV	4948	4948	.	+	.	ID=1986;Variant_seq=C;Dbxref=dbSNP_129:rs20954714;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399038.1	dbSNP	SNV	4952	4952	.	+	.	ID=1987;Variant_seq=T;Dbxref=dbSNP_129:rs20954704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399038.1	dbSNP	SNV	5630	5630	.	+	.	ID=1988;Variant_seq=T;Dbxref=dbSNP_129:rs20952624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398727.1	dbSNP	SNV	219	219	.	+	.	ID=1989;Variant_seq=A;Dbxref=dbSNP_129:rs54200949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398727.1	dbSNP	SNV	223	223	.	+	.	ID=1990;Variant_seq=A;Dbxref=dbSNP_129:rs53866247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398727.1	dbSNP	SNV	242	242	.	+	.	ID=1991;Variant_seq=A;Dbxref=dbSNP_129:rs53773376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398727.1	dbSNP	SNV	244	244	.	+	.	ID=1992;Variant_seq=T;Dbxref=dbSNP_129:rs54143197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398727.1	dbSNP	SNV	245	245	.	+	.	ID=1993;Variant_seq=A;Dbxref=dbSNP_129:rs53223738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398727.1	dbSNP	SNV	2730	2730	.	+	.	ID=1994;Variant_seq=A;Dbxref=dbSNP_129:rs54200949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398727.1	dbSNP	SNV	2734	2734	.	+	.	ID=1995;Variant_seq=A;Dbxref=dbSNP_129:rs53866247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398727.1	dbSNP	SNV	2753	2753	.	+	.	ID=1996;Variant_seq=A;Dbxref=dbSNP_129:rs53773376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398727.1	dbSNP	SNV	2755	2755	.	+	.	ID=1997;Variant_seq=T;Dbxref=dbSNP_129:rs54143197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398727.1	dbSNP	SNV	2756	2756	.	+	.	ID=1998;Variant_seq=A;Dbxref=dbSNP_129:rs53223738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041889.1	dbSNP	SNV	1217	1217	.	+	.	ID=1999;Variant_seq=T;Dbxref=dbSNP_129:rs21425945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041889.1	dbSNP	SNV	1662	1662	.	+	.	ID=2000;Variant_seq=T;Dbxref=dbSNP_129:rs53615975;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049985.1	dbSNP	SNV	370	370	.	+	.	ID=2001;Variant_seq=T;Dbxref=dbSNP_129:rs19479271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049985.1	dbSNP	SNV	371	371	.	+	.	ID=2002;Variant_seq=C;Dbxref=dbSNP_129:rs19479261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049985.1	dbSNP	deletion	1028	1028	.	+	.	ID=2003;Variant_seq=-;Dbxref=dbSNP_129:rs53063498;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398436.1	dbSNP	SNV	2365	2365	.	+	.	ID=2004;Variant_seq=A;Dbxref=dbSNP_129:rs18101758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398436.1	dbSNP	SNV	13264	13264	.	+	.	ID=2005;Variant_seq=T;Dbxref=dbSNP_129:rs20264795;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398899.1	dbSNP	SNV	509	509	.	+	.	ID=2006;Variant_seq=T;Dbxref=dbSNP_129:rs54304522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398899.1	dbSNP	SNV	640	640	.	+	.	ID=2007;Variant_seq=A;Dbxref=dbSNP_129:rs53328017;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398899.1	dbSNP	SNV	677	677	.	+	.	ID=2008;Variant_seq=C;Dbxref=dbSNP_129:rs53210641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398899.1	dbSNP	SNV	681	681	.	+	.	ID=2009;Variant_seq=A;Dbxref=dbSNP_129:rs52906566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398899.1	dbSNP	SNV	682	682	.	+	.	ID=2010;Variant_seq=C;Dbxref=dbSNP_129:rs53184085;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398899.1	dbSNP	SNV	4336	4336	.	+	.	ID=2011;Variant_seq=T;Dbxref=dbSNP_129:rs54400105;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398899.1	dbSNP	SNV	4854	4854	.	+	.	ID=2012;Variant_seq=A;Dbxref=dbSNP_129:rs54095583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398899.1	dbSNP	SNV	6471	6471	.	+	.	ID=2013;Variant_seq=A;Dbxref=dbSNP_129:rs54383380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398899.1	dbSNP	SNV	6902	6902	.	+	.	ID=2014;Variant_seq=G;Dbxref=dbSNP_129:rs20407272;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398495.1	dbSNP	SNV	11864	11864	.	+	.	ID=2015;Variant_seq=A;Dbxref=dbSNP_129:rs18282439;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398495.1	dbSNP	SNV	13260	13260	.	+	.	ID=2016;Variant_seq=C;Dbxref=dbSNP_129:rs54250419;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400781.1	dbSNP	SNV	1630	1630	.	+	.	ID=2017;Variant_seq=T;Dbxref=dbSNP_129:rs18841263;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400781.1	dbSNP	SNV	1636	1636	.	+	.	ID=2018;Variant_seq=C;Dbxref=dbSNP_129:rs18841273;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	2973	2973	.	+	.	ID=2019;Variant_seq=C;Dbxref=dbSNP_129:rs20539132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042235.1	dbSNP	SNV	3224	3224	.	+	.	ID=2020;Variant_seq=C;Dbxref=dbSNP_129:rs20539292;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	3272	3272	.	+	.	ID=2021;Variant_seq=A;Dbxref=dbSNP_129:rs20539332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042235.1	dbSNP	SNV	3303	3303	.	+	.	ID=2022;Variant_seq=A;Dbxref=dbSNP_129:rs20539342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042235.1	dbSNP	SNV	3310	3310	.	+	.	ID=2023;Variant_seq=T;Dbxref=dbSNP_129:rs20539352;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042235.1	dbSNP	SNV	3341	3341	.	+	.	ID=2024;Variant_seq=A;Dbxref=dbSNP_129:rs20539372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042235.1	dbSNP	SNV	3470	3470	.	+	.	ID=2025;Variant_seq=G;Dbxref=dbSNP_129:rs20539404;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042235.1	dbSNP	SNV	3476	3476	.	+	.	ID=2026;Variant_seq=C;Dbxref=dbSNP_129:rs20539414;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	3482	3482	.	+	.	ID=2027;Variant_seq=C;Dbxref=dbSNP_129:rs20539424;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	3620	3620	.	+	.	ID=2028;Variant_seq=T;Dbxref=dbSNP_129:rs20538942;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042235.1	dbSNP	SNV	3645	3645	.	+	.	ID=2029;Variant_seq=C;Dbxref=dbSNP_129:rs20538972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	3657	3657	.	+	.	ID=2030;Variant_seq=A;Dbxref=dbSNP_129:rs20538982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	3782	3782	.	+	.	ID=2031;Variant_seq=C;Dbxref=dbSNP_129:rs20539132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042235.1	dbSNP	SNV	4033	4033	.	+	.	ID=2032;Variant_seq=C;Dbxref=dbSNP_129:rs20539292;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042235.1	dbSNP	SNV	4081	4081	.	+	.	ID=2033;Variant_seq=A;Dbxref=dbSNP_129:rs20539332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049855.1	dbSNP	SNV	184	184	.	+	.	ID=2034;Variant_seq=T;Dbxref=dbSNP_129:rs20304962;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046039.1	dbSNP	SNV	249	249	.	+	.	ID=2035;Variant_seq=C;Dbxref=dbSNP_129:rs20902985;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046039.1	dbSNP	SNV	251	251	.	+	.	ID=2036;Variant_seq=C;Dbxref=dbSNP_129:rs20902995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046039.1	dbSNP	SNV	1084	1084	.	+	.	ID=2037;Variant_seq=G;Dbxref=dbSNP_129:rs20903115;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	474	474	.	+	.	ID=2038;Variant_seq=T;Dbxref=dbSNP_129:rs52890888;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	525	525	.	+	.	ID=2039;Variant_seq=T;Dbxref=dbSNP_129:rs53633383;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	5937	5937	.	+	.	ID=2040;Variant_seq=A;Dbxref=dbSNP_129:rs21216484;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	9670	9670	.	+	.	ID=2041;Variant_seq=A;Dbxref=dbSNP_129:rs53821744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	9749	9749	.	+	.	ID=2042;Variant_seq=T;Dbxref=dbSNP_129:rs18389420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	9790	9790	.	+	.	ID=2043;Variant_seq=A;Dbxref=dbSNP_129:rs53863963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	10148	10148	.	+	.	ID=2044;Variant_seq=T;Dbxref=dbSNP_129:rs53633383;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	10199	10199	.	+	.	ID=2045;Variant_seq=T;Dbxref=dbSNP_129:rs52890888;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	11710	11710	.	+	.	ID=2046;Variant_seq=G;Dbxref=dbSNP_129:rs54223555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	11719	11719	.	+	.	ID=2047;Variant_seq=C;Dbxref=dbSNP_129:rs52868562;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	11742	11742	.	+	.	ID=2048;Variant_seq=T;Dbxref=dbSNP_129:rs53842044;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	11746	11746	.	+	.	ID=2049;Variant_seq=T;Dbxref=dbSNP_129:rs53929328;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	11748	11748	.	+	.	ID=2050;Variant_seq=G;Dbxref=dbSNP_129:rs53668818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	11758	11758	.	+	.	ID=2051;Variant_seq=A;Dbxref=dbSNP_129:rs53887796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	11782	11782	.	+	.	ID=2052;Variant_seq=A;Dbxref=dbSNP_129:rs53906561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	11791	11791	.	+	.	ID=2053;Variant_seq=C;Dbxref=dbSNP_129:rs54199421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	11796	11796	.	+	.	ID=2054;Variant_seq=T;Dbxref=dbSNP_129:rs54373593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	11797	11797	.	+	.	ID=2055;Variant_seq=T;Dbxref=dbSNP_129:rs53291954;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	12108	12108	.	+	.	ID=2056;Variant_seq=T;Dbxref=dbSNP_129:rs19096653;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	29321	29321	.	+	.	ID=2057;Variant_seq=A;Dbxref=dbSNP_129:rs18883388;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	29330	29330	.	+	.	ID=2058;Variant_seq=A;Dbxref=dbSNP_129:rs18883398;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	29352	29352	.	+	.	ID=2059;Variant_seq=G;Dbxref=dbSNP_129:rs18883428;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	29371	29371	.	+	.	ID=2060;Variant_seq=T;Dbxref=dbSNP_129:rs18883438;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	29628	29628	.	+	.	ID=2061;Variant_seq=A;Dbxref=dbSNP_129:rs18883541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	29714	29714	.	+	.	ID=2062;Variant_seq=G;Dbxref=dbSNP_129:rs18883581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	29733	29733	.	+	.	ID=2063;Variant_seq=T;Dbxref=dbSNP_129:rs18883601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	29740	29740	.	+	.	ID=2064;Variant_seq=C;Dbxref=dbSNP_129:rs18883611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	29743	29743	.	+	.	ID=2065;Variant_seq=T;Dbxref=dbSNP_129:rs18883631;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	29753	29753	.	+	.	ID=2066;Variant_seq=G;Dbxref=dbSNP_129:rs18883641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	29764	29764	.	+	.	ID=2067;Variant_seq=C;Dbxref=dbSNP_129:rs18883651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	29772	29772	.	+	.	ID=2068;Variant_seq=G;Dbxref=dbSNP_129:rs18883661;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	29775	29775	.	+	.	ID=2069;Variant_seq=A;Dbxref=dbSNP_129:rs18883671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	29807	29807	.	+	.	ID=2070;Variant_seq=C;Dbxref=dbSNP_129:rs18883691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	29808	29808	.	+	.	ID=2071;Variant_seq=C;Dbxref=dbSNP_129:rs18883701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	34334	34334	.	+	.	ID=2072;Variant_seq=G;Dbxref=dbSNP_129:rs53817091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	34343	34343	.	+	.	ID=2073;Variant_seq=C;Dbxref=dbSNP_129:rs54043648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	40697	40697	.	+	.	ID=2074;Variant_seq=G;Dbxref=dbSNP_129:rs20911577;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	42713	42713	.	+	.	ID=2075;Variant_seq=G;Dbxref=dbSNP_129:rs19658979;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	49292	49292	.	+	.	ID=2076;Variant_seq=C;Dbxref=dbSNP_129:rs52961771;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52376	52376	.	+	.	ID=2077;Variant_seq=G;Dbxref=dbSNP_129:rs20911917;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	52380	52380	.	+	.	ID=2078;Variant_seq=A;Dbxref=dbSNP_129:rs20911927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	52381	52381	.	+	.	ID=2079;Variant_seq=A;Dbxref=dbSNP_129:rs20911937;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	52394	52394	.	+	.	ID=2080;Variant_seq=G;Dbxref=dbSNP_129:rs20911947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	52397	52397	.	+	.	ID=2081;Variant_seq=G;Dbxref=dbSNP_129:rs20911957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	52400	52400	.	+	.	ID=2082;Variant_seq=G;Dbxref=dbSNP_129:rs20911967;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52402	52402	.	+	.	ID=2083;Variant_seq=T;Dbxref=dbSNP_129:rs20911977;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	52405	52405	.	+	.	ID=2084;Variant_seq=T;Dbxref=dbSNP_129:rs20911987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	52407	52407	.	+	.	ID=2085;Variant_seq=C;Dbxref=dbSNP_129:rs20911997;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52421	52421	.	+	.	ID=2086;Variant_seq=C;Dbxref=dbSNP_129:rs20912007;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52430	52430	.	+	.	ID=2087;Variant_seq=T;Dbxref=dbSNP_129:rs20912027;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	52441	52441	.	+	.	ID=2088;Variant_seq=T;Dbxref=dbSNP_129:rs20912037;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	52442	52442	.	+	.	ID=2089;Variant_seq=T;Dbxref=dbSNP_129:rs20912047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	52587	52587	.	+	.	ID=2090;Variant_seq=A;Dbxref=dbSNP_129:rs20912307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52590	52590	.	+	.	ID=2091;Variant_seq=T;Dbxref=dbSNP_129:rs20912317;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	52594	52594	.	+	.	ID=2092;Variant_seq=C;Dbxref=dbSNP_129:rs20912327;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52598	52598	.	+	.	ID=2093;Variant_seq=C;Dbxref=dbSNP_129:rs20912338;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52612	52612	.	+	.	ID=2094;Variant_seq=A;Dbxref=dbSNP_129:rs20912348;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52613	52613	.	+	.	ID=2095;Variant_seq=C;Dbxref=dbSNP_129:rs20912358;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398245.1	dbSNP	SNV	52633	52633	.	+	.	ID=2096;Variant_seq=A;Dbxref=dbSNP_129:rs20912378;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	52653	52653	.	+	.	ID=2097;Variant_seq=A;Dbxref=dbSNP_129:rs20912388;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398245.1	dbSNP	SNV	53967	53967	.	+	.	ID=2098;Variant_seq=C;Dbxref=dbSNP_129:rs53361925;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	54062	54062	.	+	.	ID=2099;Variant_seq=G;Dbxref=dbSNP_129:rs52944090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	54086	54086	.	+	.	ID=2100;Variant_seq=A,T;Dbxref=dbSNP_129:rs53003970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	55498	55498	.	+	.	ID=2101;Variant_seq=G;Dbxref=dbSNP_129:rs19024329;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	55499	55499	.	+	.	ID=2102;Variant_seq=T;Dbxref=dbSNP_129:rs19024339;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398245.1	dbSNP	SNV	55502	55502	.	+	.	ID=2103;Variant_seq=T;Dbxref=dbSNP_129:rs19024349;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398245.1	dbSNP	SNV	55504	55504	.	+	.	ID=2104;Variant_seq=A;Dbxref=dbSNP_129:rs19024359;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048975.1	dbSNP	SNV	1310	1310	.	+	.	ID=2105;Variant_seq=G;Dbxref=dbSNP_129:rs53269041;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041015.1	dbSNP	SNV	2144	2144	.	+	.	ID=2106;Variant_seq=A;Dbxref=dbSNP_129:rs53675191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044267.1	dbSNP	SNV	2991	2991	.	+	.	ID=2107;Variant_seq=A;Dbxref=dbSNP_129:rs21263561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398375.1	dbSNP	SNV	13604	13604	.	+	.	ID=2108;Variant_seq=C;Dbxref=dbSNP_129:rs19062883;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398375.1	dbSNP	SNV	14560	14560	.	+	.	ID=2109;Variant_seq=C;Dbxref=dbSNP_129:rs21473328;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398375.1	dbSNP	SNV	15280	15280	.	+	.	ID=2110;Variant_seq=A;Dbxref=dbSNP_129:rs21506390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040235.1	dbSNP	SNV	1527	1527	.	+	.	ID=2111;Variant_seq=C;Dbxref=dbSNP_129:rs19272207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040235.1	dbSNP	SNV	1771	1771	.	+	.	ID=2112;Variant_seq=T;Dbxref=dbSNP_129:rs19272107;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040235.1	dbSNP	SNV	1773	1773	.	+	.	ID=2113;Variant_seq=C;Dbxref=dbSNP_129:rs19272097;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040235.1	dbSNP	SNV	1785	1785	.	+	.	ID=2114;Variant_seq=G;Dbxref=dbSNP_129:rs19272087;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040235.1	dbSNP	SNV	1787	1787	.	+	.	ID=2115;Variant_seq=A;Dbxref=dbSNP_129:rs19272077;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040235.1	dbSNP	SNV	1820	1820	.	+	.	ID=2116;Variant_seq=G;Dbxref=dbSNP_129:rs19272067;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040235.1	dbSNP	SNV	2186	2186	.	+	.	ID=2117;Variant_seq=T;Dbxref=dbSNP_129:rs19271937;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040235.1	dbSNP	SNV	2191	2191	.	+	.	ID=2118;Variant_seq=T;Dbxref=dbSNP_129:rs19271927;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040235.1	dbSNP	SNV	3946	3946	.	+	.	ID=2119;Variant_seq=A;Dbxref=dbSNP_129:rs54028302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398940.1	dbSNP	SNV	512	512	.	+	.	ID=2120;Variant_seq=G;Dbxref=dbSNP_129:rs19246388;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398940.1	dbSNP	SNV	5480	5480	.	+	.	ID=2121;Variant_seq=T;Dbxref=dbSNP_129:rs19979424;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043793.1	dbSNP	SNV	1465	1465	.	+	.	ID=2122;Variant_seq=G;Dbxref=dbSNP_129:rs20591762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049460.1	dbSNP	SNV	1083	1083	.	+	.	ID=2123;Variant_seq=G;Dbxref=dbSNP_129:rs19431366;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049460.1	dbSNP	SNV	1085	1085	.	+	.	ID=2124;Variant_seq=A;Dbxref=dbSNP_129:rs19431376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1097	1097	.	+	.	ID=2125;Variant_seq=G;Dbxref=dbSNP_129:rs19431386;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049460.1	dbSNP	SNV	1106	1106	.	+	.	ID=2126;Variant_seq=C;Dbxref=dbSNP_129:rs19431406;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1230	1230	.	+	.	ID=2127;Variant_seq=T;Dbxref=dbSNP_129:rs19431416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049460.1	dbSNP	SNV	1275	1275	.	+	.	ID=2128;Variant_seq=T;Dbxref=dbSNP_129:rs19431426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049460.1	dbSNP	SNV	1279	1279	.	+	.	ID=2129;Variant_seq=T;Dbxref=dbSNP_129:rs19431436;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049460.1	dbSNP	SNV	1310	1310	.	+	.	ID=2130;Variant_seq=A;Dbxref=dbSNP_129:rs19431446;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049460.1	dbSNP	SNV	1311	1311	.	+	.	ID=2131;Variant_seq=A;Dbxref=dbSNP_129:rs19431456;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1315	1315	.	+	.	ID=2132;Variant_seq=T;Dbxref=dbSNP_129:rs19431466;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049460.1	dbSNP	SNV	1324	1324	.	+	.	ID=2133;Variant_seq=G;Dbxref=dbSNP_129:rs19431486;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049460.1	dbSNP	SNV	1424	1424	.	+	.	ID=2134;Variant_seq=A;Dbxref=dbSNP_129:rs19431526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049460.1	dbSNP	SNV	1485	1485	.	+	.	ID=2135;Variant_seq=T;Dbxref=dbSNP_129:rs19431556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049460.1	dbSNP	SNV	1500	1500	.	+	.	ID=2136;Variant_seq=C;Dbxref=dbSNP_129:rs19431576;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1501	1501	.	+	.	ID=2137;Variant_seq=A;Dbxref=dbSNP_129:rs19431586;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1505	1505	.	+	.	ID=2138;Variant_seq=C;Dbxref=dbSNP_129:rs19431596;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1512	1512	.	+	.	ID=2139;Variant_seq=C;Dbxref=dbSNP_129:rs19431616;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049460.1	dbSNP	SNV	1532	1532	.	+	.	ID=2140;Variant_seq=T;Dbxref=dbSNP_129:rs19431636;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049460.1	dbSNP	SNV	1538	1538	.	+	.	ID=2141;Variant_seq=C;Dbxref=dbSNP_129:rs19431646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049460.1	dbSNP	SNV	1801	1801	.	+	.	ID=2142;Variant_seq=A;Dbxref=dbSNP_129:rs18766050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398766.1	dbSNP	SNV	337	337	.	+	.	ID=2143;Variant_seq=T;Dbxref=dbSNP_129:rs18764512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398766.1	dbSNP	SNV	345	345	.	+	.	ID=2144;Variant_seq=T;Dbxref=dbSNP_129:rs18764521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	350	350	.	+	.	ID=2145;Variant_seq=A;Dbxref=dbSNP_129:rs18764530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	373	373	.	+	.	ID=2146;Variant_seq=A;Dbxref=dbSNP_129:rs18764548;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	400	400	.	+	.	ID=2147;Variant_seq=A;Dbxref=dbSNP_129:rs18764594;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	401	401	.	+	.	ID=2148;Variant_seq=T;Dbxref=dbSNP_129:rs18764603;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	406	406	.	+	.	ID=2149;Variant_seq=T;Dbxref=dbSNP_129:rs18764612;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	431	431	.	+	.	ID=2150;Variant_seq=T;Dbxref=dbSNP_129:rs18764630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	438	438	.	+	.	ID=2151;Variant_seq=T;Dbxref=dbSNP_129:rs18764639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	440	440	.	+	.	ID=2152;Variant_seq=A;Dbxref=dbSNP_129:rs18764648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	447	447	.	+	.	ID=2153;Variant_seq=G;Dbxref=dbSNP_129:rs18764657;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	453	453	.	+	.	ID=2154;Variant_seq=A;Dbxref=dbSNP_129:rs18764666;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	480	480	.	+	.	ID=2155;Variant_seq=C;Dbxref=dbSNP_129:rs18764693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	1228	1228	.	+	.	ID=2156;Variant_seq=G;Dbxref=dbSNP_129:rs18764991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398766.1	dbSNP	SNV	1274	1274	.	+	.	ID=2157;Variant_seq=C;Dbxref=dbSNP_129:rs18765036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	8966	8966	.	+	.	ID=2158;Variant_seq=C;Dbxref=dbSNP_129:rs20255245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	9437	9437	.	+	.	ID=2159;Variant_seq=T;Dbxref=dbSNP_129:rs53172748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	9448	9448	.	+	.	ID=2160;Variant_seq=T;Dbxref=dbSNP_129:rs52977203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398766.1	dbSNP	SNV	9464	9464	.	+	.	ID=2161;Variant_seq=A;Dbxref=dbSNP_129:rs53587962;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	9467	9467	.	+	.	ID=2162;Variant_seq=A;Dbxref=dbSNP_129:rs54039913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398766.1	dbSNP	SNV	9476	9476	.	+	.	ID=2163;Variant_seq=C;Dbxref=dbSNP_129:rs53241202;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398766.1	dbSNP	SNV	9484	9484	.	+	.	ID=2164;Variant_seq=C;Dbxref=dbSNP_129:rs53265974;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398766.1	dbSNP	SNV	9491	9491	.	+	.	ID=2165;Variant_seq=A;Dbxref=dbSNP_129:rs53257660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400676.1	dbSNP	SNV	228	228	.	+	.	ID=2166;Variant_seq=G;Dbxref=dbSNP_129:rs18086258;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400676.1	dbSNP	SNV	253	253	.	+	.	ID=2167;Variant_seq=C;Dbxref=dbSNP_129:rs18086303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400676.1	dbSNP	SNV	265	265	.	+	.	ID=2168;Variant_seq=C;Dbxref=dbSNP_129:rs18086914;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2317	2317	.	+	.	ID=2169;Variant_seq=T;Dbxref=dbSNP_129:rs53375364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400676.1	dbSNP	SNV	2320	2320	.	+	.	ID=2170;Variant_seq=G;Dbxref=dbSNP_129:rs53252797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2325	2325	.	+	.	ID=2171;Variant_seq=T;Dbxref=dbSNP_129:rs54334625;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400676.1	dbSNP	SNV	2355	2355	.	+	.	ID=2172;Variant_seq=A;Dbxref=dbSNP_129:rs54235133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400676.1	dbSNP	SNV	2358	2358	.	+	.	ID=2173;Variant_seq=C;Dbxref=dbSNP_129:rs52929550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400676.1	dbSNP	SNV	2363	2363	.	+	.	ID=2174;Variant_seq=T;Dbxref=dbSNP_129:rs53091399;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2371	2371	.	+	.	ID=2175;Variant_seq=C;Dbxref=dbSNP_129:rs53306565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400676.1	dbSNP	SNV	2373	2373	.	+	.	ID=2176;Variant_seq=G;Dbxref=dbSNP_129:rs53608010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2487	2487	.	+	.	ID=2177;Variant_seq=G;Dbxref=dbSNP_129:rs52864827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2499	2499	.	+	.	ID=2178;Variant_seq=A;Dbxref=dbSNP_129:rs53572516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400676.1	dbSNP	SNV	2546	2546	.	+	.	ID=2179;Variant_seq=G;Dbxref=dbSNP_129:rs54145836;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400676.1	dbSNP	SNV	2547	2547	.	+	.	ID=2180;Variant_seq=T;Dbxref=dbSNP_129:rs53372228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1035	1035	.	+	.	ID=2181;Variant_seq=C;Dbxref=dbSNP_129:rs53378680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	1041	1041	.	+	.	ID=2182;Variant_seq=G;Dbxref=dbSNP_129:rs53712199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	insertion	1047	1047	.	+	.	ID=2183;Variant_seq=A;Dbxref=dbSNP_129:rs52855766;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH398286.1	dbSNP	deletion	1052	1052	.	+	.	ID=2184;Variant_seq=-;Dbxref=dbSNP_129:rs54115111;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1184	1184	.	+	.	ID=2185;Variant_seq=G;Dbxref=dbSNP_129:rs54105553;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	1198	1198	.	+	.	ID=2186;Variant_seq=G;Dbxref=dbSNP_129:rs53893266;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	1208	1208	.	+	.	ID=2187;Variant_seq=T;Dbxref=dbSNP_129:rs53927210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1402	1402	.	+	.	ID=2188;Variant_seq=C;Dbxref=dbSNP_129:rs53538978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398286.1	dbSNP	SNV	1566	1566	.	+	.	ID=2189;Variant_seq=G;Dbxref=dbSNP_129:rs19804334;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1568	1568	.	+	.	ID=2190;Variant_seq=G;Dbxref=dbSNP_129:rs19804331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1570	1570	.	+	.	ID=2191;Variant_seq=C;Dbxref=dbSNP_129:rs19804328;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	1573	1573	.	+	.	ID=2192;Variant_seq=T;Dbxref=dbSNP_129:rs19804325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	1725	1725	.	+	.	ID=2193;Variant_seq=T;Dbxref=dbSNP_129:rs53370096;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	1734	1734	.	+	.	ID=2194;Variant_seq=G;Dbxref=dbSNP_129:rs53966636;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	1791	1791	.	+	.	ID=2195;Variant_seq=A;Dbxref=dbSNP_129:rs53819926;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	1792	1792	.	+	.	ID=2196;Variant_seq=A;Dbxref=dbSNP_129:rs52889233;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	2402	2402	.	+	.	ID=2197;Variant_seq=A;Dbxref=dbSNP_129:rs54072314;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	2403	2403	.	+	.	ID=2198;Variant_seq=G;Dbxref=dbSNP_129:rs52941742;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	2423	2423	.	+	.	ID=2199;Variant_seq=A;Dbxref=dbSNP_129:rs53809650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	deletion	2424	2424	.	+	.	ID=2200;Variant_seq=-;Dbxref=dbSNP_129:rs54146201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	deletion	2427	2427	.	+	.	ID=2201;Variant_seq=-;Dbxref=dbSNP_129:rs53751604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	2431	2431	.	+	.	ID=2202;Variant_seq=T;Dbxref=dbSNP_129:rs53445370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	2434	2434	.	+	.	ID=2203;Variant_seq=T;Dbxref=dbSNP_129:rs53083136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398286.1	dbSNP	SNV	2450	2450	.	+	.	ID=2204;Variant_seq=T;Dbxref=dbSNP_129:rs53720229;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398286.1	dbSNP	SNV	2458	2458	.	+	.	ID=2205;Variant_seq=A;Dbxref=dbSNP_129:rs54176432;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398286.1	dbSNP	SNV	2483	2483	.	+	.	ID=2206;Variant_seq=T;Dbxref=dbSNP_129:rs54359206;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398286.1	dbSNP	SNV	2489	2489	.	+	.	ID=2207;Variant_seq=G;Dbxref=dbSNP_129:rs53560483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	4029	4029	.	+	.	ID=2208;Variant_seq=A;Dbxref=dbSNP_129:rs18272796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	4032	4032	.	+	.	ID=2209;Variant_seq=A;Dbxref=dbSNP_129:rs18272787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	4070	4070	.	+	.	ID=2210;Variant_seq=C;Dbxref=dbSNP_129:rs18272769;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398399.1	dbSNP	SNV	4100	4100	.	+	.	ID=2211;Variant_seq=T;Dbxref=dbSNP_129:rs18272760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	4117	4117	.	+	.	ID=2212;Variant_seq=A;Dbxref=dbSNP_129:rs18272751;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	4176	4176	.	+	.	ID=2213;Variant_seq=C;Dbxref=dbSNP_129:rs18272715;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398399.1	dbSNP	SNV	4232	4232	.	+	.	ID=2214;Variant_seq=T;Dbxref=dbSNP_129:rs18272688;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	11306	11306	.	+	.	ID=2215;Variant_seq=A;Dbxref=dbSNP_129:rs17904090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	12121	12121	.	+	.	ID=2216;Variant_seq=A;Dbxref=dbSNP_129:rs19086935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	14001	14001	.	+	.	ID=2217;Variant_seq=T;Dbxref=dbSNP_129:rs18685752;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	14779	14779	.	+	.	ID=2218;Variant_seq=T;Dbxref=dbSNP_129:rs18407990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	15232	15232	.	+	.	ID=2219;Variant_seq=T;Dbxref=dbSNP_129:rs21275745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	16455	16455	.	+	.	ID=2220;Variant_seq=T;Dbxref=dbSNP_129:rs53256822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398399.1	dbSNP	SNV	19417	19417	.	+	.	ID=2221;Variant_seq=A;Dbxref=dbSNP_129:rs21276055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	19669	19669	.	+	.	ID=2222;Variant_seq=A;Dbxref=dbSNP_129:rs17935999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398399.1	dbSNP	SNV	20021	20021	.	+	.	ID=2223;Variant_seq=A;Dbxref=dbSNP_129:rs21276135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042911.1	dbSNP	SNV	3501	3501	.	+	.	ID=2224;Variant_seq=T;Dbxref=dbSNP_129:rs19297123;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042911.1	dbSNP	SNV	3611	3611	.	+	.	ID=2225;Variant_seq=A;Dbxref=dbSNP_129:rs19086303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042911.1	dbSNP	SNV	3622	3622	.	+	.	ID=2226;Variant_seq=A;Dbxref=dbSNP_129:rs19086333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042911.1	dbSNP	SNV	3633	3633	.	+	.	ID=2227;Variant_seq=G;Dbxref=dbSNP_129:rs19086343;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041391.1	dbSNP	SNV	1164	1164	.	+	.	ID=2228;Variant_seq=T;Dbxref=dbSNP_129:rs21778456;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041391.1	dbSNP	SNV	3858	3858	.	+	.	ID=2229;Variant_seq=T;Dbxref=dbSNP_129:rs53088381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045048.1	dbSNP	SNV	372	372	.	+	.	ID=2230;Variant_seq=G;Dbxref=dbSNP_129:rs21129753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399748.1	dbSNP	SNV	2735	2735	.	+	.	ID=2231;Variant_seq=T;Dbxref=dbSNP_129:rs19131958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041891.1	dbSNP	SNV	2357	2357	.	+	.	ID=2232;Variant_seq=C;Dbxref=dbSNP_129:rs20849343;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041891.1	dbSNP	SNV	2363	2363	.	+	.	ID=2233;Variant_seq=A;Dbxref=dbSNP_129:rs20849333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399717.1	dbSNP	insertion	1227	1227	.	+	.	ID=2234;Variant_seq=C;Dbxref=dbSNP_129:rs53897545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH398312.1	dbSNP	SNV	4532	4532	.	+	.	ID=2235;Variant_seq=T;Dbxref=dbSNP_129:rs52851294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398312.1	dbSNP	SNV	7661	7661	.	+	.	ID=2236;Variant_seq=C;Dbxref=dbSNP_129:rs20341161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398312.1	dbSNP	SNV	7798	7798	.	+	.	ID=2237;Variant_seq=G;Dbxref=dbSNP_129:rs20341171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398312.1	dbSNP	SNV	17598	17598	.	+	.	ID=2238;Variant_seq=A;Dbxref=dbSNP_129:rs53024574;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398312.1	dbSNP	SNV	21226	21226	.	+	.	ID=2239;Variant_seq=T;Dbxref=dbSNP_129:rs53190651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398312.1	dbSNP	SNV	21226	21226	.	+	.	ID=2240;Variant_seq=T;Dbxref=dbSNP_129:rs18849781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398312.1	dbSNP	SNV	21230	21230	.	+	.	ID=2241;Variant_seq=G;Dbxref=dbSNP_129:rs53758718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398312.1	dbSNP	SNV	21231	21231	.	+	.	ID=2242;Variant_seq=C;Dbxref=dbSNP_129:rs53727988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398312.1	dbSNP	SNV	24897	24897	.	+	.	ID=2243;Variant_seq=C;Dbxref=dbSNP_129:rs53034939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044257.1	dbSNP	SNV	805	805	.	+	.	ID=2244;Variant_seq=A;Dbxref=dbSNP_129:rs53008728;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044257.1	dbSNP	SNV	816	816	.	+	.	ID=2245;Variant_seq=G;Dbxref=dbSNP_129:rs53306507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044257.1	dbSNP	SNV	1104	1104	.	+	.	ID=2246;Variant_seq=C;Dbxref=dbSNP_129:rs21182762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044257.1	dbSNP	SNV	2352	2352	.	+	.	ID=2247;Variant_seq=G;Dbxref=dbSNP_129:rs18581873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044257.1	dbSNP	SNV	2358	2358	.	+	.	ID=2248;Variant_seq=T;Dbxref=dbSNP_129:rs18581864;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044257.1	dbSNP	SNV	2359	2359	.	+	.	ID=2249;Variant_seq=T;Dbxref=dbSNP_129:rs18581855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044257.1	dbSNP	SNV	3054	3054	.	+	.	ID=2250;Variant_seq=A;Dbxref=dbSNP_129:rs52893068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041928.1	dbSNP	SNV	1029	1029	.	+	.	ID=2251;Variant_seq=G;Dbxref=dbSNP_129:rs53712730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041928.1	dbSNP	SNV	3444	3444	.	+	.	ID=2252;Variant_seq=C;Dbxref=dbSNP_129:rs18508731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043165.1	dbSNP	SNV	210	210	.	+	.	ID=2253;Variant_seq=C;Dbxref=dbSNP_129:rs53386210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043165.1	dbSNP	SNV	1431	1431	.	+	.	ID=2254;Variant_seq=A;Dbxref=dbSNP_129:rs18615266;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	303	303	.	+	.	ID=2255;Variant_seq=T;Dbxref=dbSNP_129:rs19600644;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	649	649	.	+	.	ID=2256;Variant_seq=A;Dbxref=dbSNP_129:rs18312719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	1288	1288	.	+	.	ID=2257;Variant_seq=T;Dbxref=dbSNP_129:rs18312890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	1466	1466	.	+	.	ID=2258;Variant_seq=A;Dbxref=dbSNP_129:rs18312953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037415.1	dbSNP	SNV	2064	2064	.	+	.	ID=2259;Variant_seq=T;Dbxref=dbSNP_129:rs53301518;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	2072	2072	.	+	.	ID=2260;Variant_seq=T;Dbxref=dbSNP_129:rs53688881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	2758	2758	.	+	.	ID=2261;Variant_seq=A;Dbxref=dbSNP_129:rs18313115;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037415.1	dbSNP	SNV	3504	3504	.	+	.	ID=2262;Variant_seq=T;Dbxref=dbSNP_129:rs19940839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	4671	4671	.	+	.	ID=2263;Variant_seq=T;Dbxref=dbSNP_129:rs54239128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	5404	5404	.	+	.	ID=2264;Variant_seq=A;Dbxref=dbSNP_129:rs19940379;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	5595	5595	.	+	.	ID=2265;Variant_seq=A;Dbxref=dbSNP_129:rs19940309;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	8540	8540	.	+	.	ID=2266;Variant_seq=A;Dbxref=dbSNP_129:rs52998224;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	9109	9109	.	+	.	ID=2267;Variant_seq=T;Dbxref=dbSNP_129:rs21057449;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	10424	10424	.	+	.	ID=2268;Variant_seq=C;Dbxref=dbSNP_129:rs19548620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037415.1	dbSNP	SNV	10430	10430	.	+	.	ID=2269;Variant_seq=T;Dbxref=dbSNP_129:rs19548630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	10448	10448	.	+	.	ID=2270;Variant_seq=G;Dbxref=dbSNP_129:rs19548650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037415.1	dbSNP	SNV	10474	10474	.	+	.	ID=2271;Variant_seq=T;Dbxref=dbSNP_129:rs19548660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	10526	10526	.	+	.	ID=2272;Variant_seq=T;Dbxref=dbSNP_129:rs19742213;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037415.1	dbSNP	SNV	10544	10544	.	+	.	ID=2273;Variant_seq=G;Dbxref=dbSNP_129:rs19548690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037415.1	dbSNP	SNV	10552	10552	.	+	.	ID=2274;Variant_seq=G;Dbxref=dbSNP_129:rs19548700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037415.1	dbSNP	SNV	10624	10624	.	+	.	ID=2275;Variant_seq=T;Dbxref=dbSNP_129:rs19548710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037415.1	dbSNP	SNV	10667	10667	.	+	.	ID=2276;Variant_seq=T;Dbxref=dbSNP_129:rs19548720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046482.1	dbSNP	SNV	1821	1821	.	+	.	ID=2277;Variant_seq=A;Dbxref=dbSNP_129:rs19056928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043212.1	dbSNP	SNV	3315	3315	.	+	.	ID=2278;Variant_seq=A;Dbxref=dbSNP_129:rs53029199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043212.1	dbSNP	SNV	3317	3317	.	+	.	ID=2279;Variant_seq=T;Dbxref=dbSNP_129:rs53430628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043142.1	dbSNP	SNV	3155	3155	.	+	.	ID=2280;Variant_seq=T;Dbxref=dbSNP_129:rs53897337;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043142.1	dbSNP	SNV	3433	3433	.	+	.	ID=2281;Variant_seq=A;Dbxref=dbSNP_129:rs53354142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043142.1	dbSNP	SNV	3492	3492	.	+	.	ID=2282;Variant_seq=C;Dbxref=dbSNP_129:rs53472924;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399581.1	dbSNP	SNV	3232	3232	.	+	.	ID=2283;Variant_seq=G;Dbxref=dbSNP_129:rs19182517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045667.1	dbSNP	SNV	178	178	.	+	.	ID=2284;Variant_seq=G;Dbxref=dbSNP_129:rs20681451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045667.1	dbSNP	SNV	181	181	.	+	.	ID=2285;Variant_seq=G;Dbxref=dbSNP_129:rs20681441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045667.1	dbSNP	SNV	222	222	.	+	.	ID=2286;Variant_seq=T;Dbxref=dbSNP_129:rs20681421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045667.1	dbSNP	SNV	236	236	.	+	.	ID=2287;Variant_seq=G;Dbxref=dbSNP_129:rs20681411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045667.1	dbSNP	SNV	241	241	.	+	.	ID=2288;Variant_seq=A;Dbxref=dbSNP_129:rs20681401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045667.1	dbSNP	SNV	261	261	.	+	.	ID=2289;Variant_seq=A;Dbxref=dbSNP_129:rs20681391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045667.1	dbSNP	SNV	268	268	.	+	.	ID=2290;Variant_seq=A;Dbxref=dbSNP_129:rs20681381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045667.1	dbSNP	SNV	506	506	.	+	.	ID=2291;Variant_seq=C;Dbxref=dbSNP_129:rs20681331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045667.1	dbSNP	SNV	627	627	.	+	.	ID=2292;Variant_seq=A;Dbxref=dbSNP_129:rs20681241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039893.1	dbSNP	SNV	1933	1933	.	+	.	ID=2293;Variant_seq=G;Dbxref=dbSNP_129:rs53664138;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039893.1	dbSNP	SNV	2884	2884	.	+	.	ID=2294;Variant_seq=T;Dbxref=dbSNP_129:rs20831010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049110.1	dbSNP	SNV	345	345	.	+	.	ID=2295;Variant_seq=C;Dbxref=dbSNP_129:rs21034877;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049110.1	dbSNP	SNV	798	798	.	+	.	ID=2296;Variant_seq=T;Dbxref=dbSNP_129:rs20715515;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049110.1	dbSNP	SNV	819	819	.	+	.	ID=2297;Variant_seq=T;Dbxref=dbSNP_129:rs20715495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	825	825	.	+	.	ID=2298;Variant_seq=T;Dbxref=dbSNP_129:rs20715485;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049110.1	dbSNP	SNV	826	826	.	+	.	ID=2299;Variant_seq=A;Dbxref=dbSNP_129:rs20715475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1015	1015	.	+	.	ID=2300;Variant_seq=A;Dbxref=dbSNP_129:rs20715265;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1024	1024	.	+	.	ID=2301;Variant_seq=A;Dbxref=dbSNP_129:rs20715255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1029	1029	.	+	.	ID=2302;Variant_seq=A;Dbxref=dbSNP_129:rs20715245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1031	1031	.	+	.	ID=2303;Variant_seq=G;Dbxref=dbSNP_129:rs20715235;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049110.1	dbSNP	SNV	1035	1035	.	+	.	ID=2304;Variant_seq=G;Dbxref=dbSNP_129:rs20715225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049110.1	dbSNP	SNV	1053	1053	.	+	.	ID=2305;Variant_seq=A;Dbxref=dbSNP_129:rs20715205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1078	1078	.	+	.	ID=2306;Variant_seq=A;Dbxref=dbSNP_129:rs20715195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1079	1079	.	+	.	ID=2307;Variant_seq=C;Dbxref=dbSNP_129:rs20715185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049110.1	dbSNP	SNV	1184	1184	.	+	.	ID=2308;Variant_seq=A;Dbxref=dbSNP_129:rs53990997;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049110.1	dbSNP	SNV	1245	1245	.	+	.	ID=2309;Variant_seq=T;Dbxref=dbSNP_129:rs53877051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049110.1	dbSNP	SNV	1306	1306	.	+	.	ID=2310;Variant_seq=T;Dbxref=dbSNP_129:rs54262774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398430.1	dbSNP	SNV	13878	13878	.	+	.	ID=2311;Variant_seq=T;Dbxref=dbSNP_129:rs53138683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398430.1	dbSNP	deletion	13881	13881	.	+	.	ID=2312;Variant_seq=-;Dbxref=dbSNP_129:rs53414321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398430.1	dbSNP	SNV	13884	13884	.	+	.	ID=2313;Variant_seq=C;Dbxref=dbSNP_129:rs53122592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398430.1	dbSNP	SNV	13885	13885	.	+	.	ID=2314;Variant_seq=C;Dbxref=dbSNP_129:rs53204802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398430.1	dbSNP	SNV	17616	17616	.	+	.	ID=2315;Variant_seq=T;Dbxref=dbSNP_129:rs20163641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398430.1	dbSNP	SNV	17617	17617	.	+	.	ID=2316;Variant_seq=A;Dbxref=dbSNP_129:rs20163631;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398430.1	dbSNP	SNV	17618	17618	.	+	.	ID=2317;Variant_seq=C;Dbxref=dbSNP_129:rs20163621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398430.1	dbSNP	SNV	17619	17619	.	+	.	ID=2318;Variant_seq=T;Dbxref=dbSNP_129:rs20163611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398430.1	dbSNP	SNV	17621	17621	.	+	.	ID=2319;Variant_seq=T;Dbxref=dbSNP_129:rs20163601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398430.1	dbSNP	SNV	17624	17624	.	+	.	ID=2320;Variant_seq=C;Dbxref=dbSNP_129:rs20163591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398430.1	dbSNP	SNV	17634	17634	.	+	.	ID=2321;Variant_seq=T;Dbxref=dbSNP_129:rs20163581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398430.1	dbSNP	SNV	17640	17640	.	+	.	ID=2322;Variant_seq=A;Dbxref=dbSNP_129:rs20163561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399737.1	dbSNP	SNV	2967	2967	.	+	.	ID=2323;Variant_seq=T;Dbxref=dbSNP_129:rs19486430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399737.1	dbSNP	SNV	3820	3820	.	+	.	ID=2324;Variant_seq=G;Dbxref=dbSNP_129:rs20917257;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399737.1	dbSNP	SNV	3829	3829	.	+	.	ID=2325;Variant_seq=C;Dbxref=dbSNP_129:rs20917247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399737.1	dbSNP	SNV	3832	3832	.	+	.	ID=2326;Variant_seq=T;Dbxref=dbSNP_129:rs20917237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399737.1	dbSNP	SNV	3865	3865	.	+	.	ID=2327;Variant_seq=C;Dbxref=dbSNP_129:rs20917207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399737.1	dbSNP	SNV	3866	3866	.	+	.	ID=2328;Variant_seq=T;Dbxref=dbSNP_129:rs20917197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047945.1	dbSNP	SNV	169	169	.	+	.	ID=2329;Variant_seq=T;Dbxref=dbSNP_129:rs20783932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047945.1	dbSNP	SNV	190	190	.	+	.	ID=2330;Variant_seq=A;Dbxref=dbSNP_129:rs20470518;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047945.1	dbSNP	SNV	1028	1028	.	+	.	ID=2331;Variant_seq=T;Dbxref=dbSNP_129:rs17973128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047945.1	dbSNP	SNV	1092	1092	.	+	.	ID=2332;Variant_seq=G;Dbxref=dbSNP_129:rs21770489;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036299.1	dbSNP	SNV	911	911	.	+	.	ID=2333;Variant_seq=T;Dbxref=dbSNP_129:rs19820792;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036299.1	dbSNP	SNV	4253	4253	.	+	.	ID=2334;Variant_seq=T;Dbxref=dbSNP_129:rs18765499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036299.1	dbSNP	SNV	4263	4263	.	+	.	ID=2335;Variant_seq=T;Dbxref=dbSNP_129:rs18765508;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036299.1	dbSNP	SNV	5316	5316	.	+	.	ID=2336;Variant_seq=C;Dbxref=dbSNP_129:rs20445061;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036299.1	dbSNP	SNV	7220	7220	.	+	.	ID=2337;Variant_seq=G;Dbxref=dbSNP_129:rs18542693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036299.1	dbSNP	SNV	7492	7492	.	+	.	ID=2338;Variant_seq=G;Dbxref=dbSNP_129:rs21185660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043271.1	dbSNP	SNV	1961	1961	.	+	.	ID=2339;Variant_seq=G;Dbxref=dbSNP_129:rs21345886;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043271.1	dbSNP	SNV	2301	2301	.	+	.	ID=2340;Variant_seq=A;Dbxref=dbSNP_129:rs21547505;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043271.1	dbSNP	SNV	2520	2520	.	+	.	ID=2341;Variant_seq=T;Dbxref=dbSNP_129:rs19040167;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043271.1	dbSNP	SNV	2631	2631	.	+	.	ID=2342;Variant_seq=A;Dbxref=dbSNP_129:rs54126431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043271.1	dbSNP	SNV	2638	2638	.	+	.	ID=2343;Variant_seq=T;Dbxref=dbSNP_129:rs54291011;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401090.1	dbSNP	SNV	1958	1958	.	+	.	ID=2344;Variant_seq=A;Dbxref=dbSNP_129:rs19788131;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038260.1	dbSNP	SNV	1274	1274	.	+	.	ID=2345;Variant_seq=T;Dbxref=dbSNP_129:rs20852565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038260.1	dbSNP	SNV	1884	1884	.	+	.	ID=2346;Variant_seq=T;Dbxref=dbSNP_129:rs20925918;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038260.1	dbSNP	SNV	4991	4991	.	+	.	ID=2347;Variant_seq=G;Dbxref=dbSNP_129:rs20158418;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040638.1	dbSNP	SNV	1098	1098	.	+	.	ID=2348;Variant_seq=A;Dbxref=dbSNP_129:rs21012866;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040638.1	dbSNP	SNV	1208	1208	.	+	.	ID=2349;Variant_seq=T;Dbxref=dbSNP_129:rs21012976;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040638.1	dbSNP	SNV	1221	1221	.	+	.	ID=2350;Variant_seq=G;Dbxref=dbSNP_129:rs21012996;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040638.1	dbSNP	SNV	1235	1235	.	+	.	ID=2351;Variant_seq=T;Dbxref=dbSNP_129:rs21013016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040638.1	dbSNP	SNV	1236	1236	.	+	.	ID=2352;Variant_seq=C;Dbxref=dbSNP_129:rs21013026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040638.1	dbSNP	SNV	1239	1239	.	+	.	ID=2353;Variant_seq=T;Dbxref=dbSNP_129:rs21013036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040638.1	dbSNP	SNV	1250	1250	.	+	.	ID=2354;Variant_seq=A;Dbxref=dbSNP_129:rs21013046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	3906	3906	.	+	.	ID=2355;Variant_seq=T;Dbxref=dbSNP_129:rs19500240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	9604	9604	.	+	.	ID=2356;Variant_seq=A;Dbxref=dbSNP_129:rs18174241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	11100	11100	.	+	.	ID=2357;Variant_seq=T;Dbxref=dbSNP_129:rs19816556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	14042	14042	.	+	.	ID=2358;Variant_seq=A;Dbxref=dbSNP_129:rs20749517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	15549	15549	.	+	.	ID=2359;Variant_seq=G;Dbxref=dbSNP_129:rs19752726;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	16008	16008	.	+	.	ID=2360;Variant_seq=T;Dbxref=dbSNP_129:rs19187904;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	16009	16009	.	+	.	ID=2361;Variant_seq=T;Dbxref=dbSNP_129:rs19187894;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	16011	16011	.	+	.	ID=2362;Variant_seq=G;Dbxref=dbSNP_129:rs19187884;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	16012	16012	.	+	.	ID=2363;Variant_seq=C;Dbxref=dbSNP_129:rs19187874;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	17367	17367	.	+	.	ID=2364;Variant_seq=A;Dbxref=dbSNP_129:rs53318129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	21449	21449	.	+	.	ID=2365;Variant_seq=A;Dbxref=dbSNP_129:rs54014203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	21521	21521	.	+	.	ID=2366;Variant_seq=A;Dbxref=dbSNP_129:rs52982737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	21548	21548	.	+	.	ID=2367;Variant_seq=C;Dbxref=dbSNP_129:rs54026170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	21552	21552	.	+	.	ID=2368;Variant_seq=C;Dbxref=dbSNP_129:rs54316135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	21586	21586	.	+	.	ID=2369;Variant_seq=T;Dbxref=dbSNP_129:rs53834149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	21600	21600	.	+	.	ID=2370;Variant_seq=A;Dbxref=dbSNP_129:rs54169983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	21602	21602	.	+	.	ID=2371;Variant_seq=A;Dbxref=dbSNP_129:rs54113338;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398303.1	dbSNP	SNV	22065	22065	.	+	.	ID=2372;Variant_seq=T;Dbxref=dbSNP_129:rs54218282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	22168	22168	.	+	.	ID=2373;Variant_seq=T;Dbxref=dbSNP_129:rs53611898;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	22194	22194	.	+	.	ID=2374;Variant_seq=T;Dbxref=dbSNP_129:rs52966727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	22195	22195	.	+	.	ID=2375;Variant_seq=C;Dbxref=dbSNP_129:rs54119468;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	24038	24038	.	+	.	ID=2376;Variant_seq=G;Dbxref=dbSNP_129:rs19179375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	24040	24040	.	+	.	ID=2377;Variant_seq=T;Dbxref=dbSNP_129:rs19179365;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	24041	24041	.	+	.	ID=2378;Variant_seq=G;Dbxref=dbSNP_129:rs19179355;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398303.1	dbSNP	SNV	24046	24046	.	+	.	ID=2379;Variant_seq=T;Dbxref=dbSNP_129:rs19179345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398303.1	dbSNP	SNV	24047	24047	.	+	.	ID=2380;Variant_seq=T;Dbxref=dbSNP_129:rs19179335;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398303.1	dbSNP	SNV	24048	24048	.	+	.	ID=2381;Variant_seq=C;Dbxref=dbSNP_129:rs19179325;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	SNV	1194	1194	.	+	.	ID=2382;Variant_seq=C;Dbxref=dbSNP_129:rs53457192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	SNV	1243	1243	.	+	.	ID=2383;Variant_seq=T;Dbxref=dbSNP_129:rs54162261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	1318	1318	.	+	.	ID=2384;Variant_seq=A;Dbxref=dbSNP_129:rs53039859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	1318	1318	.	+	.	ID=2385;Variant_seq=A;Dbxref=dbSNP_129:rs53965619;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	1322	1322	.	+	.	ID=2386;Variant_seq=G;Dbxref=dbSNP_129:rs54125731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	SNV	1328	1328	.	+	.	ID=2387;Variant_seq=T;Dbxref=dbSNP_129:rs53628220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	1333	1333	.	+	.	ID=2388;Variant_seq=C;Dbxref=dbSNP_129:rs53536358;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	SNV	1843	1843	.	+	.	ID=2389;Variant_seq=G;Dbxref=dbSNP_129:rs53857236;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044943.1	dbSNP	SNV	1846	1846	.	+	.	ID=2390;Variant_seq=A;Dbxref=dbSNP_129:rs54304311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	1856	1856	.	+	.	ID=2391;Variant_seq=T;Dbxref=dbSNP_129:rs53287427;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	1857	1857	.	+	.	ID=2392;Variant_seq=A;Dbxref=dbSNP_129:rs53752670;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	1860	1860	.	+	.	ID=2393;Variant_seq=T;Dbxref=dbSNP_129:rs52993203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	1866	1866	.	+	.	ID=2394;Variant_seq=G;Dbxref=dbSNP_129:rs53876249;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	deletion	1895	1896	.	+	.	ID=2395;Variant_seq=-;Dbxref=dbSNP_129:rs53469569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TC
AAAA02044943.1	dbSNP	SNV	1896	1896	.	+	.	ID=2396;Variant_seq=T;Dbxref=dbSNP_129:rs54216206;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	1897	1897	.	+	.	ID=2397;Variant_seq=C;Dbxref=dbSNP_129:rs53894720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044943.1	dbSNP	deletion	1900	1901	.	+	.	ID=2398;Variant_seq=-;Dbxref=dbSNP_129:rs53099403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TT
AAAA02044943.1	dbSNP	deletion	1903	1903	.	+	.	ID=2399;Variant_seq=-;Dbxref=dbSNP_129:rs53792891;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044943.1	dbSNP	SNV	1907	1907	.	+	.	ID=2400;Variant_seq=C;Dbxref=dbSNP_129:rs53749333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044943.1	dbSNP	deletion	1907	1909	.	+	.	ID=2401;Variant_seq=-;Dbxref=dbSNP_129:rs54342667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TCT
AAAA02044943.1	dbSNP	SNV	1910	1910	.	+	.	ID=2402;Variant_seq=A;Dbxref=dbSNP_129:rs53103205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	1911	1911	.	+	.	ID=2403;Variant_seq=G;Dbxref=dbSNP_129:rs53914745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044943.1	dbSNP	SNV	1912	1912	.	+	.	ID=2404;Variant_seq=T;Dbxref=dbSNP_129:rs53299740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044943.1	dbSNP	SNV	2843	2843	.	+	.	ID=2405;Variant_seq=G;Dbxref=dbSNP_129:rs53662448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044943.1	dbSNP	SNV	2851	2851	.	+	.	ID=2406;Variant_seq=A;Dbxref=dbSNP_129:rs53073217;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399620.1	dbSNP	SNV	2957	2957	.	+	.	ID=2407;Variant_seq=G;Dbxref=dbSNP_129:rs53017184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399620.1	dbSNP	SNV	3101	3101	.	+	.	ID=2408;Variant_seq=T;Dbxref=dbSNP_129:rs18097585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399620.1	dbSNP	SNV	3980	3980	.	+	.	ID=2409;Variant_seq=G;Dbxref=dbSNP_129:rs54303416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399620.1	dbSNP	SNV	3983	3983	.	+	.	ID=2410;Variant_seq=G;Dbxref=dbSNP_129:rs53997484;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399620.1	dbSNP	SNV	4100	4100	.	+	.	ID=2411;Variant_seq=T;Dbxref=dbSNP_129:rs53128835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048210.1	dbSNP	SNV	552	552	.	+	.	ID=2412;Variant_seq=G;Dbxref=dbSNP_129:rs21505480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048210.1	dbSNP	SNV	658	658	.	+	.	ID=2413;Variant_seq=T;Dbxref=dbSNP_129:rs19059695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048210.1	dbSNP	SNV	669	669	.	+	.	ID=2414;Variant_seq=T;Dbxref=dbSNP_129:rs19059705;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048210.1	dbSNP	SNV	1364	1364	.	+	.	ID=2415;Variant_seq=A;Dbxref=dbSNP_129:rs19060244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048210.1	dbSNP	SNV	2112	2112	.	+	.	ID=2416;Variant_seq=A;Dbxref=dbSNP_129:rs19060671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048210.1	dbSNP	SNV	2127	2127	.	+	.	ID=2417;Variant_seq=C;Dbxref=dbSNP_129:rs19060690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035746.1	dbSNP	SNV	21567	21567	.	+	.	ID=2418;Variant_seq=A;Dbxref=dbSNP_129:rs20648390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399309.1	dbSNP	SNV	1101	1101	.	+	.	ID=2419;Variant_seq=A;Dbxref=dbSNP_129:rs53610818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399309.1	dbSNP	SNV	4690	4690	.	+	.	ID=2420;Variant_seq=C;Dbxref=dbSNP_129:rs53610818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043392.1	dbSNP	SNV	760	760	.	+	.	ID=2421;Variant_seq=A;Dbxref=dbSNP_129:rs52893354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043392.1	dbSNP	SNV	2365	2365	.	+	.	ID=2422;Variant_seq=T;Dbxref=dbSNP_129:rs21586876;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043392.1	dbSNP	SNV	3000	3000	.	+	.	ID=2423;Variant_seq=G;Dbxref=dbSNP_129:rs19106212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043636.1	dbSNP	SNV	2133	2133	.	+	.	ID=2424;Variant_seq=C;Dbxref=dbSNP_129:rs21618502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043636.1	dbSNP	SNV	2306	2306	.	+	.	ID=2425;Variant_seq=G;Dbxref=dbSNP_129:rs21618493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043636.1	dbSNP	SNV	2360	2360	.	+	.	ID=2426;Variant_seq=G;Dbxref=dbSNP_129:rs21618484;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043636.1	dbSNP	SNV	2421	2421	.	+	.	ID=2427;Variant_seq=G;Dbxref=dbSNP_129:rs21618475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043636.1	dbSNP	SNV	2542	2542	.	+	.	ID=2428;Variant_seq=C;Dbxref=dbSNP_129:rs21618448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400147.1	dbSNP	SNV	1262	1262	.	+	.	ID=2429;Variant_seq=A,C,G;Dbxref=dbSNP_129:rs17888320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400147.1	dbSNP	SNV	1877	1877	.	+	.	ID=2430;Variant_seq=C;Dbxref=dbSNP_129:rs19643616;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398541.1	dbSNP	SNV	580	580	.	+	.	ID=2431;Variant_seq=A;Dbxref=dbSNP_129:rs18340829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398541.1	dbSNP	SNV	613	613	.	+	.	ID=2432;Variant_seq=G;Dbxref=dbSNP_129:rs52929948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398541.1	dbSNP	SNV	623	623	.	+	.	ID=2433;Variant_seq=T;Dbxref=dbSNP_129:rs53441391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398541.1	dbSNP	SNV	637	637	.	+	.	ID=2434;Variant_seq=C;Dbxref=dbSNP_129:rs53198107;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398541.1	dbSNP	SNV	650	650	.	+	.	ID=2435;Variant_seq=G;Dbxref=dbSNP_129:rs54390915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398541.1	dbSNP	SNV	674	674	.	+	.	ID=2436;Variant_seq=G;Dbxref=dbSNP_129:rs53214204;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398541.1	dbSNP	SNV	723	723	.	+	.	ID=2437;Variant_seq=C;Dbxref=dbSNP_129:rs53061603;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398541.1	dbSNP	SNV	3857	3857	.	+	.	ID=2438;Variant_seq=C;Dbxref=dbSNP_129:rs53956623;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398541.1	dbSNP	SNV	5120	5120	.	+	.	ID=2439;Variant_seq=A;Dbxref=dbSNP_129:rs53076217;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398541.1	dbSNP	SNV	5146	5146	.	+	.	ID=2440;Variant_seq=T;Dbxref=dbSNP_129:rs53935061;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398541.1	dbSNP	SNV	5219	5219	.	+	.	ID=2441;Variant_seq=C;Dbxref=dbSNP_129:rs53703213;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398541.1	dbSNP	SNV	8429	8429	.	+	.	ID=2442;Variant_seq=A;Dbxref=dbSNP_129:rs54074737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398541.1	dbSNP	SNV	11402	11402	.	+	.	ID=2443;Variant_seq=T;Dbxref=dbSNP_129:rs18773986;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398541.1	dbSNP	SNV	12707	12707	.	+	.	ID=2444;Variant_seq=C;Dbxref=dbSNP_129:rs20215789;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046427.1	dbSNP	SNV	653	653	.	+	.	ID=2445;Variant_seq=T;Dbxref=dbSNP_129:rs54340544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	43	43	.	+	.	ID=2446;Variant_seq=T;Dbxref=dbSNP_129:rs18586506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	206	206	.	+	.	ID=2447;Variant_seq=C;Dbxref=dbSNP_129:rs18586515;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044899.1	dbSNP	SNV	213	213	.	+	.	ID=2448;Variant_seq=G;Dbxref=dbSNP_129:rs18586524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	482	482	.	+	.	ID=2449;Variant_seq=G;Dbxref=dbSNP_129:rs18586533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044899.1	dbSNP	SNV	553	553	.	+	.	ID=2450;Variant_seq=T;Dbxref=dbSNP_129:rs53829224;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	561	561	.	+	.	ID=2451;Variant_seq=T;Dbxref=dbSNP_129:rs54373605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044899.1	dbSNP	SNV	650	650	.	+	.	ID=2452;Variant_seq=T;Dbxref=dbSNP_129:rs54108252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	678	678	.	+	.	ID=2453;Variant_seq=T;Dbxref=dbSNP_129:rs18586551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	886	886	.	+	.	ID=2454;Variant_seq=C;Dbxref=dbSNP_129:rs18586578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044899.1	dbSNP	SNV	894	894	.	+	.	ID=2455;Variant_seq=A;Dbxref=dbSNP_129:rs18586587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	1323	1323	.	+	.	ID=2456;Variant_seq=C;Dbxref=dbSNP_129:rs18586623;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044899.1	dbSNP	SNV	1575	1575	.	+	.	ID=2457;Variant_seq=T;Dbxref=dbSNP_129:rs18586641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044899.1	dbSNP	SNV	1837	1837	.	+	.	ID=2458;Variant_seq=G;Dbxref=dbSNP_129:rs18789448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044899.1	dbSNP	SNV	1871	1871	.	+	.	ID=2459;Variant_seq=A;Dbxref=dbSNP_129:rs18789439;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044899.1	dbSNP	SNV	1872	1872	.	+	.	ID=2460;Variant_seq=A;Dbxref=dbSNP_129:rs18789430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044899.1	dbSNP	SNV	2796	2796	.	+	.	ID=2461;Variant_seq=T;Dbxref=dbSNP_129:rs21255219;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044899.1	dbSNP	SNV	2797	2797	.	+	.	ID=2462;Variant_seq=G;Dbxref=dbSNP_129:rs21255229;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044899.1	dbSNP	SNV	2907	2907	.	+	.	ID=2463;Variant_seq=A;Dbxref=dbSNP_129:rs18789403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041981.1	dbSNP	SNV	292	292	.	+	.	ID=2464;Variant_seq=A;Dbxref=dbSNP_129:rs19133899;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041981.1	dbSNP	SNV	349	349	.	+	.	ID=2465;Variant_seq=T;Dbxref=dbSNP_129:rs19133889;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041981.1	dbSNP	SNV	353	353	.	+	.	ID=2466;Variant_seq=C;Dbxref=dbSNP_129:rs19133879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041981.1	dbSNP	SNV	481	481	.	+	.	ID=2467;Variant_seq=T;Dbxref=dbSNP_129:rs19133869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041981.1	dbSNP	SNV	525	525	.	+	.	ID=2468;Variant_seq=C;Dbxref=dbSNP_129:rs19133859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041981.1	dbSNP	SNV	533	533	.	+	.	ID=2469;Variant_seq=A;Dbxref=dbSNP_129:rs19133849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041981.1	dbSNP	SNV	537	537	.	+	.	ID=2470;Variant_seq=G;Dbxref=dbSNP_129:rs19133839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041981.1	dbSNP	SNV	625	625	.	+	.	ID=2471;Variant_seq=T;Dbxref=dbSNP_129:rs19133829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041981.1	dbSNP	SNV	647	647	.	+	.	ID=2472;Variant_seq=T;Dbxref=dbSNP_129:rs19133819;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041981.1	dbSNP	SNV	664	664	.	+	.	ID=2473;Variant_seq=G;Dbxref=dbSNP_129:rs19133809;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041981.1	dbSNP	SNV	680	680	.	+	.	ID=2474;Variant_seq=T;Dbxref=dbSNP_129:rs19133779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041981.1	dbSNP	SNV	729	729	.	+	.	ID=2475;Variant_seq=T;Dbxref=dbSNP_129:rs19133769;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041981.1	dbSNP	SNV	734	734	.	+	.	ID=2476;Variant_seq=T;Dbxref=dbSNP_129:rs19133759;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041981.1	dbSNP	SNV	2517	2517	.	+	.	ID=2477;Variant_seq=T;Dbxref=dbSNP_129:rs20262727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041981.1	dbSNP	SNV	2522	2522	.	+	.	ID=2478;Variant_seq=A;Dbxref=dbSNP_129:rs20262717;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041981.1	dbSNP	SNV	2523	2523	.	+	.	ID=2479;Variant_seq=C;Dbxref=dbSNP_129:rs20262707;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040574.1	dbSNP	SNV	1330	1330	.	+	.	ID=2480;Variant_seq=G;Dbxref=dbSNP_129:rs20690171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398557.1	dbSNP	SNV	1859	1859	.	+	.	ID=2481;Variant_seq=G;Dbxref=dbSNP_129:rs52849070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398557.1	dbSNP	SNV	1861	1861	.	+	.	ID=2482;Variant_seq=A;Dbxref=dbSNP_129:rs53820812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398557.1	dbSNP	SNV	1862	1862	.	+	.	ID=2483;Variant_seq=A;Dbxref=dbSNP_129:rs54042988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398557.1	dbSNP	SNV	1864	1864	.	+	.	ID=2484;Variant_seq=G;Dbxref=dbSNP_129:rs54087302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398557.1	dbSNP	SNV	12433	12433	.	+	.	ID=2485;Variant_seq=A;Dbxref=dbSNP_129:rs21669129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398557.1	dbSNP	SNV	12482	12482	.	+	.	ID=2486;Variant_seq=T;Dbxref=dbSNP_129:rs20084185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	2475	2475	.	+	.	ID=2487;Variant_seq=T;Dbxref=dbSNP_129:rs53866323;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	2477	2477	.	+	.	ID=2488;Variant_seq=T;Dbxref=dbSNP_129:rs54291383;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	2483	2483	.	+	.	ID=2489;Variant_seq=A;Dbxref=dbSNP_129:rs53835616;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	2486	2486	.	+	.	ID=2490;Variant_seq=T;Dbxref=dbSNP_129:rs52983247;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	2624	2624	.	+	.	ID=2491;Variant_seq=T;Dbxref=dbSNP_129:rs54116940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041529.1	dbSNP	SNV	2625	2625	.	+	.	ID=2492;Variant_seq=G;Dbxref=dbSNP_129:rs52966551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041529.1	dbSNP	SNV	3796	3796	.	+	.	ID=2493;Variant_seq=A;Dbxref=dbSNP_129:rs53576791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	3819	3819	.	+	.	ID=2494;Variant_seq=T;Dbxref=dbSNP_129:rs53061917;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041529.1	dbSNP	SNV	3821	3821	.	+	.	ID=2495;Variant_seq=C;Dbxref=dbSNP_129:rs53477165;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041529.1	dbSNP	SNV	3821	3821	.	+	.	ID=2496;Variant_seq=C;Dbxref=dbSNP_129:rs54080057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041529.1	dbSNP	SNV	3826	3826	.	+	.	ID=2497;Variant_seq=T;Dbxref=dbSNP_129:rs54356160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	3829	3829	.	+	.	ID=2498;Variant_seq=T;Dbxref=dbSNP_129:rs53848628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	3830	3830	.	+	.	ID=2499;Variant_seq=T;Dbxref=dbSNP_129:rs53772454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	deletion	3831	3831	.	+	.	ID=2500;Variant_seq=-;Dbxref=dbSNP_129:rs54397968;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	3832	3832	.	+	.	ID=2501;Variant_seq=G;Dbxref=dbSNP_129:rs52897327;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041529.1	dbSNP	SNV	3833	3833	.	+	.	ID=2502;Variant_seq=A,C;Dbxref=dbSNP_129:rs52965949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041529.1	dbSNP	SNV	3845	3845	.	+	.	ID=2503;Variant_seq=A;Dbxref=dbSNP_129:rs53358530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041529.1	dbSNP	SNV	3855	3855	.	+	.	ID=2504;Variant_seq=C;Dbxref=dbSNP_129:rs54249507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	3868	3868	.	+	.	ID=2505;Variant_seq=T;Dbxref=dbSNP_129:rs53070915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041529.1	dbSNP	SNV	3871	3871	.	+	.	ID=2506;Variant_seq=A;Dbxref=dbSNP_129:rs53843171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	3873	3873	.	+	.	ID=2507;Variant_seq=C;Dbxref=dbSNP_129:rs53624907;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	3873	3873	.	+	.	ID=2508;Variant_seq=C;Dbxref=dbSNP_129:rs54239685;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041529.1	dbSNP	SNV	3879	3879	.	+	.	ID=2509;Variant_seq=A;Dbxref=dbSNP_129:rs53502214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040357.1	dbSNP	SNV	824	824	.	+	.	ID=2510;Variant_seq=C;Dbxref=dbSNP_129:rs21643157;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040357.1	dbSNP	SNV	3517	3517	.	+	.	ID=2511;Variant_seq=G;Dbxref=dbSNP_129:rs54171893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040357.1	dbSNP	SNV	3556	3556	.	+	.	ID=2512;Variant_seq=C;Dbxref=dbSNP_129:rs21256268;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040357.1	dbSNP	SNV	3588	3588	.	+	.	ID=2513;Variant_seq=G;Dbxref=dbSNP_129:rs53853909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040357.1	dbSNP	SNV	3604	3604	.	+	.	ID=2514;Variant_seq=T;Dbxref=dbSNP_129:rs54372569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040357.1	dbSNP	SNV	3610	3610	.	+	.	ID=2515;Variant_seq=T;Dbxref=dbSNP_129:rs53078261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040357.1	dbSNP	SNV	4114	4114	.	+	.	ID=2516;Variant_seq=A;Dbxref=dbSNP_129:rs18588059;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040357.1	dbSNP	SNV	4387	4387	.	+	.	ID=2517;Variant_seq=T;Dbxref=dbSNP_129:rs19560227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044103.1	dbSNP	SNV	719	719	.	+	.	ID=2518;Variant_seq=G;Dbxref=dbSNP_129:rs54016220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044103.1	dbSNP	SNV	799	799	.	+	.	ID=2519;Variant_seq=T;Dbxref=dbSNP_129:rs53472855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044103.1	dbSNP	SNV	859	859	.	+	.	ID=2520;Variant_seq=A;Dbxref=dbSNP_129:rs54030360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044103.1	dbSNP	SNV	2064	2064	.	+	.	ID=2521;Variant_seq=T;Dbxref=dbSNP_129:rs21095945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044103.1	dbSNP	SNV	2065	2065	.	+	.	ID=2522;Variant_seq=A;Dbxref=dbSNP_129:rs21095935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044103.1	dbSNP	SNV	2077	2077	.	+	.	ID=2523;Variant_seq=T;Dbxref=dbSNP_129:rs21095875;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044103.1	dbSNP	SNV	2630	2630	.	+	.	ID=2524;Variant_seq=C;Dbxref=dbSNP_129:rs21093748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044103.1	dbSNP	SNV	2631	2631	.	+	.	ID=2525;Variant_seq=C;Dbxref=dbSNP_129:rs21093738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044103.1	dbSNP	SNV	2655	2655	.	+	.	ID=2526;Variant_seq=T;Dbxref=dbSNP_129:rs21093648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044103.1	dbSNP	SNV	2657	2657	.	+	.	ID=2527;Variant_seq=C;Dbxref=dbSNP_129:rs21093638;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044103.1	dbSNP	SNV	2678	2678	.	+	.	ID=2528;Variant_seq=T;Dbxref=dbSNP_129:rs21093548;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044103.1	dbSNP	SNV	2681	2681	.	+	.	ID=2529;Variant_seq=A;Dbxref=dbSNP_129:rs21093528;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044103.1	dbSNP	SNV	2702	2702	.	+	.	ID=2530;Variant_seq=C;Dbxref=dbSNP_129:rs21093458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044103.1	dbSNP	SNV	2703	2703	.	+	.	ID=2531;Variant_seq=G;Dbxref=dbSNP_129:rs21093448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398576.1	dbSNP	SNV	207	207	.	+	.	ID=2532;Variant_seq=G;Dbxref=dbSNP_129:rs20613651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398576.1	dbSNP	SNV	336	336	.	+	.	ID=2533;Variant_seq=G;Dbxref=dbSNP_129:rs20613751;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398576.1	dbSNP	SNV	358	358	.	+	.	ID=2534;Variant_seq=A;Dbxref=dbSNP_129:rs20613761;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398576.1	dbSNP	SNV	591	591	.	+	.	ID=2535;Variant_seq=G;Dbxref=dbSNP_129:rs20613981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398576.1	dbSNP	SNV	1879	1879	.	+	.	ID=2536;Variant_seq=A;Dbxref=dbSNP_129:rs54005327;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398576.1	dbSNP	SNV	6137	6137	.	+	.	ID=2537;Variant_seq=G;Dbxref=dbSNP_129:rs19458368;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398576.1	dbSNP	SNV	7263	7263	.	+	.	ID=2538;Variant_seq=A;Dbxref=dbSNP_129:rs20577519;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398576.1	dbSNP	SNV	7271	7271	.	+	.	ID=2539;Variant_seq=A;Dbxref=dbSNP_129:rs20577509;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398576.1	dbSNP	SNV	7305	7305	.	+	.	ID=2540;Variant_seq=T;Dbxref=dbSNP_129:rs20577489;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398576.1	dbSNP	SNV	7306	7306	.	+	.	ID=2541;Variant_seq=C;Dbxref=dbSNP_129:rs20577479;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398576.1	dbSNP	SNV	7672	7672	.	+	.	ID=2542;Variant_seq=C;Dbxref=dbSNP_129:rs19971758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398576.1	dbSNP	SNV	7677	7677	.	+	.	ID=2543;Variant_seq=A;Dbxref=dbSNP_129:rs19971748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398576.1	dbSNP	SNV	7684	7684	.	+	.	ID=2544;Variant_seq=G;Dbxref=dbSNP_129:rs19971738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398576.1	dbSNP	SNV	12463	12463	.	+	.	ID=2545;Variant_seq=G;Dbxref=dbSNP_129:rs53927749;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045586.1	dbSNP	SNV	189	189	.	+	.	ID=2546;Variant_seq=A;Dbxref=dbSNP_129:rs20215869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045586.1	dbSNP	SNV	1573	1573	.	+	.	ID=2547;Variant_seq=A;Dbxref=dbSNP_129:rs53885204;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045586.1	dbSNP	deletion	2070	2071	.	+	.	ID=2548;Variant_seq=-;Dbxref=dbSNP_129:rs53747901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TT
AAAA02045586.1	dbSNP	insertion	2104	2104	.	+	.	ID=2549;Variant_seq=ATA;Dbxref=dbSNP_129:rs54171383;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
CH399850.1	dbSNP	SNV	2334	2334	.	+	.	ID=2550;Variant_seq=G;Dbxref=dbSNP_129:rs53285579;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045751.1	dbSNP	SNV	1645	1645	.	+	.	ID=2551;Variant_seq=T;Dbxref=dbSNP_129:rs20240183;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045751.1	dbSNP	SNV	1898	1898	.	+	.	ID=2552;Variant_seq=A;Dbxref=dbSNP_129:rs20240173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045751.1	dbSNP	SNV	1900	1900	.	+	.	ID=2553;Variant_seq=T;Dbxref=dbSNP_129:rs20240163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045751.1	dbSNP	SNV	2000	2000	.	+	.	ID=2554;Variant_seq=G;Dbxref=dbSNP_129:rs20240143;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045751.1	dbSNP	SNV	2005	2005	.	+	.	ID=2555;Variant_seq=C;Dbxref=dbSNP_129:rs20240133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045751.1	dbSNP	SNV	2048	2048	.	+	.	ID=2556;Variant_seq=T;Dbxref=dbSNP_129:rs20240113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045751.1	dbSNP	SNV	2136	2136	.	+	.	ID=2557;Variant_seq=A;Dbxref=dbSNP_129:rs20240083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045751.1	dbSNP	SNV	2231	2231	.	+	.	ID=2558;Variant_seq=T;Dbxref=dbSNP_129:rs20240073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045751.1	dbSNP	SNV	2342	2342	.	+	.	ID=2559;Variant_seq=G;Dbxref=dbSNP_129:rs20240053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	2028	2028	.	+	.	ID=2560;Variant_seq=T;Dbxref=dbSNP_129:rs54251945;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399144.1	dbSNP	SNV	2037	2037	.	+	.	ID=2561;Variant_seq=C;Dbxref=dbSNP_129:rs53149191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399144.1	dbSNP	SNV	2114	2114	.	+	.	ID=2562;Variant_seq=C;Dbxref=dbSNP_129:rs53461260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399144.1	dbSNP	SNV	2130	2130	.	+	.	ID=2563;Variant_seq=G;Dbxref=dbSNP_129:rs54292351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399144.1	dbSNP	SNV	2136	2136	.	+	.	ID=2564;Variant_seq=A;Dbxref=dbSNP_129:rs53468672;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399144.1	dbSNP	SNV	3017	3017	.	+	.	ID=2565;Variant_seq=T;Dbxref=dbSNP_129:rs54062587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399144.1	dbSNP	SNV	3020	3020	.	+	.	ID=2566;Variant_seq=G;Dbxref=dbSNP_129:rs53743736;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399144.1	dbSNP	SNV	3022	3022	.	+	.	ID=2567;Variant_seq=C;Dbxref=dbSNP_129:rs53787392;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399144.1	dbSNP	SNV	3024	3024	.	+	.	ID=2568;Variant_seq=T;Dbxref=dbSNP_129:rs53555208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	3058	3058	.	+	.	ID=2569;Variant_seq=G;Dbxref=dbSNP_129:rs53382914;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399144.1	dbSNP	SNV	3061	3061	.	+	.	ID=2570;Variant_seq=A;Dbxref=dbSNP_129:rs53666701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	5390	5390	.	+	.	ID=2571;Variant_seq=T;Dbxref=dbSNP_129:rs53327570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	6393	6393	.	+	.	ID=2572;Variant_seq=G;Dbxref=dbSNP_129:rs20507586;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	6541	6541	.	+	.	ID=2573;Variant_seq=A;Dbxref=dbSNP_129:rs20507566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399144.1	dbSNP	SNV	6740	6740	.	+	.	ID=2574;Variant_seq=T;Dbxref=dbSNP_129:rs20507536;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399144.1	dbSNP	SNV	6784	6784	.	+	.	ID=2575;Variant_seq=T;Dbxref=dbSNP_129:rs20507526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399263.1	dbSNP	SNV	4287	4287	.	+	.	ID=2576;Variant_seq=T;Dbxref=dbSNP_129:rs20885690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399263.1	dbSNP	SNV	4294	4294	.	+	.	ID=2577;Variant_seq=C;Dbxref=dbSNP_129:rs20885710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399263.1	dbSNP	SNV	4295	4295	.	+	.	ID=2578;Variant_seq=T;Dbxref=dbSNP_129:rs20885720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399263.1	dbSNP	SNV	4299	4299	.	+	.	ID=2579;Variant_seq=G;Dbxref=dbSNP_129:rs20885730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399263.1	dbSNP	SNV	4330	4330	.	+	.	ID=2580;Variant_seq=A;Dbxref=dbSNP_129:rs20885760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399263.1	dbSNP	SNV	4342	4342	.	+	.	ID=2581;Variant_seq=A;Dbxref=dbSNP_129:rs20885780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401128.1	dbSNP	SNV	1555	1555	.	+	.	ID=2582;Variant_seq=T;Dbxref=dbSNP_129:rs21620691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046071.1	dbSNP	SNV	70	70	.	+	.	ID=2583;Variant_seq=G;Dbxref=dbSNP_129:rs20843518;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	73	73	.	+	.	ID=2584;Variant_seq=G;Dbxref=dbSNP_129:rs20843528;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046071.1	dbSNP	SNV	79	79	.	+	.	ID=2585;Variant_seq=T;Dbxref=dbSNP_129:rs20843538;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046071.1	dbSNP	SNV	88	88	.	+	.	ID=2586;Variant_seq=G;Dbxref=dbSNP_129:rs20843550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046071.1	dbSNP	SNV	91	91	.	+	.	ID=2587;Variant_seq=T;Dbxref=dbSNP_129:rs20843559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046071.1	dbSNP	SNV	97	97	.	+	.	ID=2588;Variant_seq=C;Dbxref=dbSNP_129:rs20843579;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	100	100	.	+	.	ID=2589;Variant_seq=A;Dbxref=dbSNP_129:rs20843589;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046071.1	dbSNP	SNV	143	143	.	+	.	ID=2590;Variant_seq=A;Dbxref=dbSNP_129:rs20843619;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046071.1	dbSNP	SNV	172	172	.	+	.	ID=2591;Variant_seq=C;Dbxref=dbSNP_129:rs20843629;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	177	177	.	+	.	ID=2592;Variant_seq=C;Dbxref=dbSNP_129:rs20843639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	205	205	.	+	.	ID=2593;Variant_seq=A;Dbxref=dbSNP_129:rs20843649;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	429	429	.	+	.	ID=2594;Variant_seq=A;Dbxref=dbSNP_129:rs20843699;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046071.1	dbSNP	SNV	753	753	.	+	.	ID=2595;Variant_seq=T;Dbxref=dbSNP_129:rs52897003;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046071.1	dbSNP	SNV	1017	1017	.	+	.	ID=2596;Variant_seq=C;Dbxref=dbSNP_129:rs20332238;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400740.1	dbSNP	SNV	1356	1356	.	+	.	ID=2597;Variant_seq=G;Dbxref=dbSNP_129:rs53296431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400740.1	dbSNP	SNV	1363	1363	.	+	.	ID=2598;Variant_seq=A;Dbxref=dbSNP_129:rs54287901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400740.1	dbSNP	SNV	2485	2485	.	+	.	ID=2599;Variant_seq=A;Dbxref=dbSNP_129:rs20290192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398533.1	dbSNP	SNV	7329	7329	.	+	.	ID=2600;Variant_seq=A;Dbxref=dbSNP_129:rs53676872;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398533.1	dbSNP	SNV	7348	7348	.	+	.	ID=2601;Variant_seq=G;Dbxref=dbSNP_129:rs54297145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398533.1	dbSNP	SNV	7359	7359	.	+	.	ID=2602;Variant_seq=T;Dbxref=dbSNP_129:rs53863667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398533.1	dbSNP	SNV	9802	9802	.	+	.	ID=2603;Variant_seq=A;Dbxref=dbSNP_129:rs20858433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	9813	9813	.	+	.	ID=2604;Variant_seq=C;Dbxref=dbSNP_129:rs20858463;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	11093	11093	.	+	.	ID=2605;Variant_seq=A;Dbxref=dbSNP_129:rs20040252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398533.1	dbSNP	SNV	11105	11105	.	+	.	ID=2606;Variant_seq=C;Dbxref=dbSNP_129:rs20040212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	13005	13005	.	+	.	ID=2607;Variant_seq=C;Dbxref=dbSNP_129:rs53906813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	13007	13007	.	+	.	ID=2608;Variant_seq=C;Dbxref=dbSNP_129:rs54036754;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	13017	13017	.	+	.	ID=2609;Variant_seq=A,T;Dbxref=dbSNP_129:rs53900735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398533.1	dbSNP	SNV	13018	13018	.	+	.	ID=2610;Variant_seq=C;Dbxref=dbSNP_129:rs53981370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398533.1	dbSNP	SNV	13023	13023	.	+	.	ID=2611;Variant_seq=T;Dbxref=dbSNP_129:rs54006027;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398533.1	dbSNP	SNV	13024	13024	.	+	.	ID=2612;Variant_seq=A;Dbxref=dbSNP_129:rs54350944;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398533.1	dbSNP	SNV	13890	13890	.	+	.	ID=2613;Variant_seq=A;Dbxref=dbSNP_129:rs53676872;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398533.1	dbSNP	SNV	13909	13909	.	+	.	ID=2614;Variant_seq=G;Dbxref=dbSNP_129:rs54297145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398533.1	dbSNP	SNV	13920	13920	.	+	.	ID=2615;Variant_seq=T;Dbxref=dbSNP_129:rs53863667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399044.1	dbSNP	SNV	1343	1343	.	+	.	ID=2616;Variant_seq=C;Dbxref=dbSNP_129:rs53593629;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399044.1	dbSNP	SNV	5208	5208	.	+	.	ID=2617;Variant_seq=C;Dbxref=dbSNP_129:rs20686895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399188.1	dbSNP	SNV	4153	4153	.	+	.	ID=2618;Variant_seq=A;Dbxref=dbSNP_129:rs20702451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399188.1	dbSNP	SNV	4208	4208	.	+	.	ID=2619;Variant_seq=T;Dbxref=dbSNP_129:rs20703162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399188.1	dbSNP	SNV	4253	4253	.	+	.	ID=2620;Variant_seq=T;Dbxref=dbSNP_129:rs20703182;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399188.1	dbSNP	SNV	4580	4580	.	+	.	ID=2621;Variant_seq=G;Dbxref=dbSNP_129:rs20707294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399188.1	dbSNP	SNV	5890	5890	.	+	.	ID=2622;Variant_seq=G;Dbxref=dbSNP_129:rs20703582;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399188.1	dbSNP	SNV	6360	6360	.	+	.	ID=2623;Variant_seq=G;Dbxref=dbSNP_129:rs20703802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399194.1	dbSNP	SNV	2913	2913	.	+	.	ID=2624;Variant_seq=G;Dbxref=dbSNP_129:rs19659184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042813.1	dbSNP	SNV	2606	2606	.	+	.	ID=2625;Variant_seq=A;Dbxref=dbSNP_129:rs53882591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399875.1	dbSNP	SNV	1328	1328	.	+	.	ID=2626;Variant_seq=A;Dbxref=dbSNP_129:rs18678630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399875.1	dbSNP	SNV	1430	1430	.	+	.	ID=2627;Variant_seq=C;Dbxref=dbSNP_129:rs18678648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399875.1	dbSNP	SNV	1541	1541	.	+	.	ID=2628;Variant_seq=T;Dbxref=dbSNP_129:rs18678684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399064.1	dbSNP	SNV	1883	1883	.	+	.	ID=2629;Variant_seq=C;Dbxref=dbSNP_129:rs21783244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399064.1	dbSNP	SNV	3679	3679	.	+	.	ID=2630;Variant_seq=A;Dbxref=dbSNP_129:rs53258964;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399064.1	dbSNP	SNV	3687	3687	.	+	.	ID=2631;Variant_seq=A;Dbxref=dbSNP_129:rs54373186;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049482.1	dbSNP	SNV	724	724	.	+	.	ID=2632;Variant_seq=C;Dbxref=dbSNP_129:rs19730676;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049482.1	dbSNP	SNV	734	734	.	+	.	ID=2633;Variant_seq=T;Dbxref=dbSNP_129:rs19730666;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	746	746	.	+	.	ID=2634;Variant_seq=T;Dbxref=dbSNP_129:rs19730656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	868	868	.	+	.	ID=2635;Variant_seq=C;Dbxref=dbSNP_129:rs19730516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049482.1	dbSNP	SNV	871	871	.	+	.	ID=2636;Variant_seq=T;Dbxref=dbSNP_129:rs19730506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	872	872	.	+	.	ID=2637;Variant_seq=G;Dbxref=dbSNP_129:rs19730496;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	873	873	.	+	.	ID=2638;Variant_seq=T;Dbxref=dbSNP_129:rs19730486;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	877	877	.	+	.	ID=2639;Variant_seq=G;Dbxref=dbSNP_129:rs19730476;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049482.1	dbSNP	SNV	879	879	.	+	.	ID=2640;Variant_seq=G;Dbxref=dbSNP_129:rs19730466;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	889	889	.	+	.	ID=2641;Variant_seq=C;Dbxref=dbSNP_129:rs19730426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049482.1	dbSNP	SNV	890	890	.	+	.	ID=2642;Variant_seq=T;Dbxref=dbSNP_129:rs19730416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	892	892	.	+	.	ID=2643;Variant_seq=C;Dbxref=dbSNP_129:rs19730406;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	893	893	.	+	.	ID=2644;Variant_seq=T;Dbxref=dbSNP_129:rs19730396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049482.1	dbSNP	SNV	903	903	.	+	.	ID=2645;Variant_seq=G;Dbxref=dbSNP_129:rs19730376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	904	904	.	+	.	ID=2646;Variant_seq=T;Dbxref=dbSNP_129:rs19730366;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	945	945	.	+	.	ID=2647;Variant_seq=A;Dbxref=dbSNP_129:rs19730346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049482.1	dbSNP	SNV	947	947	.	+	.	ID=2648;Variant_seq=T;Dbxref=dbSNP_129:rs19730336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049482.1	dbSNP	SNV	958	958	.	+	.	ID=2649;Variant_seq=T;Dbxref=dbSNP_129:rs19730326;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	1108	1108	.	+	.	ID=2650;Variant_seq=G;Dbxref=dbSNP_129:rs19730266;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049482.1	dbSNP	SNV	1109	1109	.	+	.	ID=2651;Variant_seq=A;Dbxref=dbSNP_129:rs19730256;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049482.1	dbSNP	SNV	1228	1228	.	+	.	ID=2652;Variant_seq=T;Dbxref=dbSNP_129:rs19730246;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041614.1	dbSNP	SNV	602	602	.	+	.	ID=2653;Variant_seq=A;Dbxref=dbSNP_129:rs18765205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041614.1	dbSNP	SNV	801	801	.	+	.	ID=2654;Variant_seq=G;Dbxref=dbSNP_129:rs18765151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041614.1	dbSNP	SNV	3667	3667	.	+	.	ID=2655;Variant_seq=G;Dbxref=dbSNP_129:rs54177973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041614.1	dbSNP	SNV	3671	3671	.	+	.	ID=2656;Variant_seq=T;Dbxref=dbSNP_129:rs54013231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041614.1	dbSNP	SNV	3718	3718	.	+	.	ID=2657;Variant_seq=G;Dbxref=dbSNP_129:rs53596184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041614.1	dbSNP	SNV	3720	3720	.	+	.	ID=2658;Variant_seq=A;Dbxref=dbSNP_129:rs53309043;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	158	158	.	+	.	ID=2659;Variant_seq=A;Dbxref=dbSNP_129:rs20105853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	3267	3267	.	+	.	ID=2660;Variant_seq=A;Dbxref=dbSNP_129:rs18871242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	3483	3483	.	+	.	ID=2661;Variant_seq=T;Dbxref=dbSNP_129:rs19511403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041540.1	dbSNP	SNV	3484	3484	.	+	.	ID=2662;Variant_seq=A;Dbxref=dbSNP_129:rs18802991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	3619	3619	.	+	.	ID=2663;Variant_seq=A;Dbxref=dbSNP_129:rs53621838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	3626	3626	.	+	.	ID=2664;Variant_seq=T;Dbxref=dbSNP_129:rs53149045;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041540.1	dbSNP	SNV	3627	3627	.	+	.	ID=2665;Variant_seq=A;Dbxref=dbSNP_129:rs18282117;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041540.1	dbSNP	SNV	4088	4088	.	+	.	ID=2666;Variant_seq=A;Dbxref=dbSNP_129:rs19511553;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049673.1	dbSNP	SNV	381	381	.	+	.	ID=2667;Variant_seq=T;Dbxref=dbSNP_129:rs53845151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049673.1	dbSNP	SNV	397	397	.	+	.	ID=2668;Variant_seq=C;Dbxref=dbSNP_129:rs54120418;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049673.1	dbSNP	SNV	693	693	.	+	.	ID=2669;Variant_seq=A;Dbxref=dbSNP_129:rs53837186;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049673.1	dbSNP	SNV	702	702	.	+	.	ID=2670;Variant_seq=T;Dbxref=dbSNP_129:rs53745911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049673.1	dbSNP	SNV	704	704	.	+	.	ID=2671;Variant_seq=T;Dbxref=dbSNP_129:rs53102592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049673.1	dbSNP	SNV	705	705	.	+	.	ID=2672;Variant_seq=A;Dbxref=dbSNP_129:rs53938642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049673.1	dbSNP	SNV	713	713	.	+	.	ID=2673;Variant_seq=A;Dbxref=dbSNP_129:rs53713310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049673.1	dbSNP	SNV	719	719	.	+	.	ID=2674;Variant_seq=C;Dbxref=dbSNP_129:rs53435259;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049673.1	dbSNP	SNV	723	723	.	+	.	ID=2675;Variant_seq=A;Dbxref=dbSNP_129:rs52881712;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049673.1	dbSNP	SNV	757	757	.	+	.	ID=2676;Variant_seq=A;Dbxref=dbSNP_129:rs53911651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400013.1	dbSNP	SNV	747	747	.	+	.	ID=2677;Variant_seq=C;Dbxref=dbSNP_129:rs19156307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400013.1	dbSNP	SNV	754	754	.	+	.	ID=2678;Variant_seq=A;Dbxref=dbSNP_129:rs19156347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400013.1	dbSNP	SNV	3172	3172	.	+	.	ID=2679;Variant_seq=G;Dbxref=dbSNP_129:rs19641256;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041988.1	dbSNP	SNV	221	221	.	+	.	ID=2680;Variant_seq=C;Dbxref=dbSNP_129:rs53333167;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041988.1	dbSNP	SNV	393	393	.	+	.	ID=2681;Variant_seq=A;Dbxref=dbSNP_129:rs53901331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041988.1	dbSNP	SNV	409	409	.	+	.	ID=2682;Variant_seq=T;Dbxref=dbSNP_129:rs54200578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041988.1	dbSNP	SNV	412	412	.	+	.	ID=2683;Variant_seq=G;Dbxref=dbSNP_129:rs54049284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041988.1	dbSNP	SNV	422	422	.	+	.	ID=2684;Variant_seq=G;Dbxref=dbSNP_129:rs52886123;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041988.1	dbSNP	SNV	975	975	.	+	.	ID=2685;Variant_seq=G;Dbxref=dbSNP_129:rs19308797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398521.1	dbSNP	SNV	14500	14500	.	+	.	ID=2686;Variant_seq=T;Dbxref=dbSNP_129:rs19053917;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398521.1	dbSNP	SNV	14512	14512	.	+	.	ID=2687;Variant_seq=T;Dbxref=dbSNP_129:rs19053947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398521.1	dbSNP	SNV	14872	14872	.	+	.	ID=2688;Variant_seq=A;Dbxref=dbSNP_129:rs17962304;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398521.1	dbSNP	SNV	14877	14877	.	+	.	ID=2689;Variant_seq=T;Dbxref=dbSNP_129:rs19144028;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045897.1	dbSNP	SNV	653	653	.	+	.	ID=2690;Variant_seq=C;Dbxref=dbSNP_129:rs53280778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045897.1	dbSNP	SNV	659	659	.	+	.	ID=2691;Variant_seq=C;Dbxref=dbSNP_129:rs53325966;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045897.1	dbSNP	SNV	660	660	.	+	.	ID=2692;Variant_seq=C;Dbxref=dbSNP_129:rs53492820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045897.1	dbSNP	SNV	661	661	.	+	.	ID=2693;Variant_seq=G;Dbxref=dbSNP_129:rs53688232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045897.1	dbSNP	SNV	668	668	.	+	.	ID=2694;Variant_seq=T,G;Dbxref=dbSNP_129:rs53925735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045897.1	dbSNP	SNV	691	691	.	+	.	ID=2695;Variant_seq=T;Dbxref=dbSNP_129:rs53024746;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045897.1	dbSNP	SNV	692	692	.	+	.	ID=2696;Variant_seq=A;Dbxref=dbSNP_129:rs54349866;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045897.1	dbSNP	SNV	2094	2094	.	+	.	ID=2697;Variant_seq=A;Dbxref=dbSNP_129:rs54024131;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043982.1	dbSNP	SNV	1937	1937	.	+	.	ID=2698;Variant_seq=G;Dbxref=dbSNP_129:rs19000254;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045045.1	dbSNP	SNV	2734	2734	.	+	.	ID=2699;Variant_seq=C;Dbxref=dbSNP_129:rs53632152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045045.1	dbSNP	SNV	2735	2735	.	+	.	ID=2700;Variant_seq=A;Dbxref=dbSNP_129:rs53893768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043896.1	dbSNP	SNV	2075	2075	.	+	.	ID=2701;Variant_seq=T;Dbxref=dbSNP_129:rs21613394;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043896.1	dbSNP	SNV	2355	2355	.	+	.	ID=2702;Variant_seq=A;Dbxref=dbSNP_129:rs21613421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043896.1	dbSNP	SNV	3016	3016	.	+	.	ID=2703;Variant_seq=G;Dbxref=dbSNP_129:rs18220648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	828	828	.	+	.	ID=2704;Variant_seq=T;Dbxref=dbSNP_129:rs20188048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	833	833	.	+	.	ID=2705;Variant_seq=C;Dbxref=dbSNP_129:rs20188058;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	836	836	.	+	.	ID=2706;Variant_seq=T;Dbxref=dbSNP_129:rs20188088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	837	837	.	+	.	ID=2707;Variant_seq=T;Dbxref=dbSNP_129:rs20188098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	997	997	.	+	.	ID=2708;Variant_seq=T;Dbxref=dbSNP_129:rs20188689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1006	1006	.	+	.	ID=2709;Variant_seq=C;Dbxref=dbSNP_129:rs20188709;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1007	1007	.	+	.	ID=2710;Variant_seq=C;Dbxref=dbSNP_129:rs20188719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1008	1008	.	+	.	ID=2711;Variant_seq=C;Dbxref=dbSNP_129:rs20188729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1009	1009	.	+	.	ID=2712;Variant_seq=G;Dbxref=dbSNP_129:rs20188739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1017	1017	.	+	.	ID=2713;Variant_seq=A;Dbxref=dbSNP_129:rs20188779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1020	1020	.	+	.	ID=2714;Variant_seq=C;Dbxref=dbSNP_129:rs20188789;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1021	1021	.	+	.	ID=2715;Variant_seq=A;Dbxref=dbSNP_129:rs20188799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1023	1023	.	+	.	ID=2716;Variant_seq=G;Dbxref=dbSNP_129:rs20188809;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1025	1025	.	+	.	ID=2717;Variant_seq=G;Dbxref=dbSNP_129:rs20188819;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1028	1028	.	+	.	ID=2718;Variant_seq=C;Dbxref=dbSNP_129:rs20188839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1029	1029	.	+	.	ID=2719;Variant_seq=C;Dbxref=dbSNP_129:rs20188849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1030	1030	.	+	.	ID=2720;Variant_seq=G;Dbxref=dbSNP_129:rs20188859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1031	1031	.	+	.	ID=2721;Variant_seq=C;Dbxref=dbSNP_129:rs20188869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1032	1032	.	+	.	ID=2722;Variant_seq=C;Dbxref=dbSNP_129:rs20188879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1040	1040	.	+	.	ID=2723;Variant_seq=G;Dbxref=dbSNP_129:rs20188909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1041	1041	.	+	.	ID=2724;Variant_seq=A;Dbxref=dbSNP_129:rs20188919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1049	1049	.	+	.	ID=2725;Variant_seq=G;Dbxref=dbSNP_129:rs20188939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1052	1052	.	+	.	ID=2726;Variant_seq=G;Dbxref=dbSNP_129:rs20188949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1053	1053	.	+	.	ID=2727;Variant_seq=A;Dbxref=dbSNP_129:rs20188959;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1055	1055	.	+	.	ID=2728;Variant_seq=A;Dbxref=dbSNP_129:rs20188969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1056	1056	.	+	.	ID=2729;Variant_seq=G;Dbxref=dbSNP_129:rs20188979;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1057	1057	.	+	.	ID=2730;Variant_seq=A;Dbxref=dbSNP_129:rs20188989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	1058	1058	.	+	.	ID=2731;Variant_seq=G;Dbxref=dbSNP_129:rs20188999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1061	1061	.	+	.	ID=2732;Variant_seq=A;Dbxref=dbSNP_129:rs20189029;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1064	1064	.	+	.	ID=2733;Variant_seq=C;Dbxref=dbSNP_129:rs20189039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	1069	1069	.	+	.	ID=2734;Variant_seq=C;Dbxref=dbSNP_129:rs20189049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1082	1082	.	+	.	ID=2735;Variant_seq=C;Dbxref=dbSNP_129:rs20189089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1085	1085	.	+	.	ID=2736;Variant_seq=C;Dbxref=dbSNP_129:rs20189099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1088	1088	.	+	.	ID=2737;Variant_seq=T;Dbxref=dbSNP_129:rs20189129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1089	1089	.	+	.	ID=2738;Variant_seq=C;Dbxref=dbSNP_129:rs20189139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1090	1090	.	+	.	ID=2739;Variant_seq=T;Dbxref=dbSNP_129:rs20189149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1091	1091	.	+	.	ID=2740;Variant_seq=C;Dbxref=dbSNP_129:rs20189159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1100	1100	.	+	.	ID=2741;Variant_seq=C;Dbxref=dbSNP_129:rs20189189;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	1104	1104	.	+	.	ID=2742;Variant_seq=G;Dbxref=dbSNP_129:rs20189199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1105	1105	.	+	.	ID=2743;Variant_seq=C;Dbxref=dbSNP_129:rs20189209;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1112	1112	.	+	.	ID=2744;Variant_seq=T;Dbxref=dbSNP_129:rs20189239;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	1113	1113	.	+	.	ID=2745;Variant_seq=C;Dbxref=dbSNP_129:rs20189249;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1114	1114	.	+	.	ID=2746;Variant_seq=G;Dbxref=dbSNP_129:rs20189259;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1115	1115	.	+	.	ID=2747;Variant_seq=C;Dbxref=dbSNP_129:rs20189269;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1125	1125	.	+	.	ID=2748;Variant_seq=C;Dbxref=dbSNP_129:rs20189289;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1127	1127	.	+	.	ID=2749;Variant_seq=G;Dbxref=dbSNP_129:rs20189299;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1128	1128	.	+	.	ID=2750;Variant_seq=C;Dbxref=dbSNP_129:rs20189309;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1145	1145	.	+	.	ID=2751;Variant_seq=C;Dbxref=dbSNP_129:rs20189359;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1156	1156	.	+	.	ID=2752;Variant_seq=T;Dbxref=dbSNP_129:rs20189379;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1157	1157	.	+	.	ID=2753;Variant_seq=G;Dbxref=dbSNP_129:rs20189389;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1160	1160	.	+	.	ID=2754;Variant_seq=T;Dbxref=dbSNP_129:rs20189419;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1161	1161	.	+	.	ID=2755;Variant_seq=C;Dbxref=dbSNP_129:rs20189429;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1162	1162	.	+	.	ID=2756;Variant_seq=C;Dbxref=dbSNP_129:rs20189439;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1163	1163	.	+	.	ID=2757;Variant_seq=C;Dbxref=dbSNP_129:rs20189449;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1164	1164	.	+	.	ID=2758;Variant_seq=G;Dbxref=dbSNP_129:rs20189459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1176	1176	.	+	.	ID=2759;Variant_seq=G;Dbxref=dbSNP_129:rs20189499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	1318	1318	.	+	.	ID=2760;Variant_seq=T;Dbxref=dbSNP_129:rs20189858;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1326	1326	.	+	.	ID=2761;Variant_seq=A;Dbxref=dbSNP_129:rs20189878;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1334	1334	.	+	.	ID=2762;Variant_seq=G;Dbxref=dbSNP_129:rs20189908;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1339	1339	.	+	.	ID=2763;Variant_seq=G;Dbxref=dbSNP_129:rs20189938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1342	1342	.	+	.	ID=2764;Variant_seq=C;Dbxref=dbSNP_129:rs20189948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1344	1344	.	+	.	ID=2765;Variant_seq=C;Dbxref=dbSNP_129:rs20189958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1352	1352	.	+	.	ID=2766;Variant_seq=T;Dbxref=dbSNP_129:rs20189978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1353	1353	.	+	.	ID=2767;Variant_seq=C;Dbxref=dbSNP_129:rs20189988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042634.1	dbSNP	SNV	1355	1355	.	+	.	ID=2768;Variant_seq=G;Dbxref=dbSNP_129:rs20189998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042634.1	dbSNP	SNV	1356	1356	.	+	.	ID=2769;Variant_seq=C;Dbxref=dbSNP_129:rs20190008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042634.1	dbSNP	SNV	1357	1357	.	+	.	ID=2770;Variant_seq=C;Dbxref=dbSNP_129:rs20190018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042634.1	dbSNP	SNV	3579	3579	.	+	.	ID=2771;Variant_seq=T;Dbxref=dbSNP_129:rs21427351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043224.1	dbSNP	SNV	34	34	.	+	.	ID=2772;Variant_seq=T;Dbxref=dbSNP_129:rs21427351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043224.1	dbSNP	SNV	974	974	.	+	.	ID=2773;Variant_seq=G;Dbxref=dbSNP_129:rs20364498;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043224.1	dbSNP	SNV	3156	3156	.	+	.	ID=2774;Variant_seq=A;Dbxref=dbSNP_129:rs21397929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043224.1	dbSNP	SNV	3410	3410	.	+	.	ID=2775;Variant_seq=C;Dbxref=dbSNP_129:rs21397939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045918.1	dbSNP	SNV	762	762	.	+	.	ID=2776;Variant_seq=T;Dbxref=dbSNP_129:rs20686995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045170.1	dbSNP	SNV	757	757	.	+	.	ID=2777;Variant_seq=C;Dbxref=dbSNP_129:rs54165051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045170.1	dbSNP	SNV	861	861	.	+	.	ID=2778;Variant_seq=T;Dbxref=dbSNP_129:rs54331066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045170.1	dbSNP	deletion	864	866	.	+	.	ID=2779;Variant_seq=-;Dbxref=dbSNP_129:rs52947896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TTC
AAAA02045170.1	dbSNP	SNV	878	878	.	+	.	ID=2780;Variant_seq=C;Dbxref=dbSNP_129:rs20174887;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045170.1	dbSNP	SNV	2132	2132	.	+	.	ID=2781;Variant_seq=T;Dbxref=dbSNP_129:rs53277372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049050.1	dbSNP	SNV	598	598	.	+	.	ID=2782;Variant_seq=G;Dbxref=dbSNP_129:rs19817838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049050.1	dbSNP	SNV	1329	1329	.	+	.	ID=2783;Variant_seq=T;Dbxref=dbSNP_129:rs53959747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049050.1	dbSNP	SNV	1344	1344	.	+	.	ID=2784;Variant_seq=A;Dbxref=dbSNP_129:rs54108341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049050.1	dbSNP	SNV	1380	1380	.	+	.	ID=2785;Variant_seq=C;Dbxref=dbSNP_129:rs52874911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049050.1	dbSNP	SNV	1400	1400	.	+	.	ID=2786;Variant_seq=T;Dbxref=dbSNP_129:rs53316563;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399355.1	dbSNP	SNV	188	188	.	+	.	ID=2787;Variant_seq=C;Dbxref=dbSNP_129:rs20761566;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399355.1	dbSNP	SNV	260	260	.	+	.	ID=2788;Variant_seq=G;Dbxref=dbSNP_129:rs20761556;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399355.1	dbSNP	SNV	308	308	.	+	.	ID=2789;Variant_seq=T;Dbxref=dbSNP_129:rs20761546;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399355.1	dbSNP	SNV	332	332	.	+	.	ID=2790;Variant_seq=G;Dbxref=dbSNP_129:rs20761536;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399355.1	dbSNP	SNV	461	461	.	+	.	ID=2791;Variant_seq=T;Dbxref=dbSNP_129:rs20761526;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399355.1	dbSNP	SNV	621	621	.	+	.	ID=2792;Variant_seq=A;Dbxref=dbSNP_129:rs20761516;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049894.1	dbSNP	SNV	1989	1989	.	+	.	ID=2793;Variant_seq=T;Dbxref=dbSNP_129:rs20807727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039550.1	dbSNP	SNV	2127	2127	.	+	.	ID=2794;Variant_seq=A;Dbxref=dbSNP_129:rs54373289;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039550.1	dbSNP	SNV	2146	2146	.	+	.	ID=2795;Variant_seq=A;Dbxref=dbSNP_129:rs53459861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398599.1	dbSNP	SNV	194	194	.	+	.	ID=2796;Variant_seq=G;Dbxref=dbSNP_129:rs21763498;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398599.1	dbSNP	SNV	944	944	.	+	.	ID=2797;Variant_seq=A;Dbxref=dbSNP_129:rs20640333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398599.1	dbSNP	SNV	3842	3842	.	+	.	ID=2798;Variant_seq=T;Dbxref=dbSNP_129:rs20945894;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398599.1	dbSNP	SNV	5584	5584	.	+	.	ID=2799;Variant_seq=G;Dbxref=dbSNP_129:rs52915995;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398599.1	dbSNP	SNV	10511	10511	.	+	.	ID=2800;Variant_seq=T;Dbxref=dbSNP_129:rs53483773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041862.1	dbSNP	SNV	1504	1504	.	+	.	ID=2801;Variant_seq=T;Dbxref=dbSNP_129:rs21202624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041862.1	dbSNP	SNV	2161	2161	.	+	.	ID=2802;Variant_seq=A;Dbxref=dbSNP_129:rs54041796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041862.1	dbSNP	deletion	2162	2162	.	+	.	ID=2803;Variant_seq=-;Dbxref=dbSNP_129:rs54110018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041862.1	dbSNP	SNV	2164	2164	.	+	.	ID=2804;Variant_seq=T;Dbxref=dbSNP_129:rs53944667;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041862.1	dbSNP	SNV	2165	2165	.	+	.	ID=2805;Variant_seq=G;Dbxref=dbSNP_129:rs53084803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041862.1	dbSNP	SNV	2172	2172	.	+	.	ID=2806;Variant_seq=T;Dbxref=dbSNP_129:rs53392928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02041862.1	dbSNP	SNV	2175	2175	.	+	.	ID=2807;Variant_seq=C;Dbxref=dbSNP_129:rs53121073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041862.1	dbSNP	SNV	2182	2182	.	+	.	ID=2808;Variant_seq=A;Dbxref=dbSNP_129:rs53153980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041862.1	dbSNP	SNV	2183	2183	.	+	.	ID=2809;Variant_seq=G;Dbxref=dbSNP_129:rs53170145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042525.1	dbSNP	SNV	2546	2546	.	+	.	ID=2810;Variant_seq=A;Dbxref=dbSNP_129:rs20447127;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040164.1	dbSNP	SNV	671	671	.	+	.	ID=2811;Variant_seq=T;Dbxref=dbSNP_129:rs20579398;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040164.1	dbSNP	SNV	1391	1391	.	+	.	ID=2812;Variant_seq=A;Dbxref=dbSNP_129:rs20948906;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040164.1	dbSNP	SNV	2980	2980	.	+	.	ID=2813;Variant_seq=C;Dbxref=dbSNP_129:rs20948846;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040164.1	dbSNP	SNV	3586	3586	.	+	.	ID=2814;Variant_seq=A;Dbxref=dbSNP_129:rs20948826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036298.1	dbSNP	SNV	7888	7888	.	+	.	ID=2815;Variant_seq=A;Dbxref=dbSNP_129:rs54250850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036298.1	dbSNP	SNV	8412	8412	.	+	.	ID=2816;Variant_seq=C;Dbxref=dbSNP_129:rs53283822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036298.1	dbSNP	SNV	8474	8474	.	+	.	ID=2817;Variant_seq=G;Dbxref=dbSNP_129:rs52868811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036298.1	dbSNP	SNV	9009	9009	.	+	.	ID=2818;Variant_seq=C;Dbxref=dbSNP_129:rs18976073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036298.1	dbSNP	SNV	10098	10098	.	+	.	ID=2819;Variant_seq=G;Dbxref=dbSNP_129:rs21690063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036298.1	dbSNP	SNV	10817	10817	.	+	.	ID=2820;Variant_seq=T;Dbxref=dbSNP_129:rs18969245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036298.1	dbSNP	SNV	10932	10932	.	+	.	ID=2821;Variant_seq=A;Dbxref=dbSNP_129:rs18146982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036298.1	dbSNP	SNV	15143	15143	.	+	.	ID=2822;Variant_seq=T;Dbxref=dbSNP_129:rs19724588;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036298.1	dbSNP	SNV	15144	15144	.	+	.	ID=2823;Variant_seq=G;Dbxref=dbSNP_129:rs19724578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036298.1	dbSNP	SNV	15269	15269	.	+	.	ID=2824;Variant_seq=A;Dbxref=dbSNP_129:rs19724558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036298.1	dbSNP	SNV	16742	16742	.	+	.	ID=2825;Variant_seq=C;Dbxref=dbSNP_129:rs19724208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036298.1	dbSNP	SNV	17272	17272	.	+	.	ID=2826;Variant_seq=T;Dbxref=dbSNP_129:rs19724138;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045217.1	dbSNP	SNV	1647	1647	.	+	.	ID=2827;Variant_seq=T;Dbxref=dbSNP_129:rs18039119;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039443.1	dbSNP	SNV	50	50	.	+	.	ID=2828;Variant_seq=C;Dbxref=dbSNP_129:rs20890972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1043	1043	.	+	.	ID=2829;Variant_seq=G;Dbxref=dbSNP_129:rs53792307;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1047	1047	.	+	.	ID=2830;Variant_seq=A;Dbxref=dbSNP_129:rs54005480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1051	1051	.	+	.	ID=2831;Variant_seq=A;Dbxref=dbSNP_129:rs54072155;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1066	1066	.	+	.	ID=2832;Variant_seq=A;Dbxref=dbSNP_129:rs54161171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1074	1074	.	+	.	ID=2833;Variant_seq=T;Dbxref=dbSNP_129:rs54022473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1075	1075	.	+	.	ID=2834;Variant_seq=A;Dbxref=dbSNP_129:rs53916065;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1080	1080	.	+	.	ID=2835;Variant_seq=A;Dbxref=dbSNP_129:rs53506506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1087	1087	.	+	.	ID=2836;Variant_seq=A;Dbxref=dbSNP_129:rs19533294;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1088	1088	.	+	.	ID=2837;Variant_seq=T;Dbxref=dbSNP_129:rs54261893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1103	1103	.	+	.	ID=2838;Variant_seq=C;Dbxref=dbSNP_129:rs53028169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1399	1399	.	+	.	ID=2839;Variant_seq=G;Dbxref=dbSNP_129:rs53395320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1399	1399	.	+	.	ID=2840;Variant_seq=C;Dbxref=dbSNP_129:rs53594391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1402	1402	.	+	.	ID=2841;Variant_seq=T;Dbxref=dbSNP_129:rs54047665;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1407	1407	.	+	.	ID=2842;Variant_seq=G;Dbxref=dbSNP_129:rs54096371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1408	1408	.	+	.	ID=2843;Variant_seq=T;Dbxref=dbSNP_129:rs52950717;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1408	1408	.	+	.	ID=2844;Variant_seq=A;Dbxref=dbSNP_129:rs53586052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1411	1411	.	+	.	ID=2845;Variant_seq=G;Dbxref=dbSNP_129:rs53067024;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1414	1414	.	+	.	ID=2846;Variant_seq=C;Dbxref=dbSNP_129:rs53546004;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1455	1455	.	+	.	ID=2847;Variant_seq=C;Dbxref=dbSNP_129:rs53956060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1464	1464	.	+	.	ID=2848;Variant_seq=G;Dbxref=dbSNP_129:rs53458257;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	SNV	1469	1469	.	+	.	ID=2849;Variant_seq=A;Dbxref=dbSNP_129:rs53905900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1469	1469	.	+	.	ID=2850;Variant_seq=T;Dbxref=dbSNP_129:rs53788958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1477	1477	.	+	.	ID=2851;Variant_seq=A;Dbxref=dbSNP_129:rs53977211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1486	1486	.	+	.	ID=2852;Variant_seq=A;Dbxref=dbSNP_129:rs53286888;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1488	1488	.	+	.	ID=2853;Variant_seq=A;Dbxref=dbSNP_129:rs53342175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1488	1488	.	+	.	ID=2854;Variant_seq=T;Dbxref=dbSNP_129:rs54196349;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1496	1496	.	+	.	ID=2855;Variant_seq=T;Dbxref=dbSNP_129:rs53693984;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1497	1497	.	+	.	ID=2856;Variant_seq=C;Dbxref=dbSNP_129:rs54179965;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1504	1504	.	+	.	ID=2857;Variant_seq=A;Dbxref=dbSNP_129:rs53727697;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1506	1506	.	+	.	ID=2858;Variant_seq=A;Dbxref=dbSNP_129:rs54222158;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1507	1507	.	+	.	ID=2859;Variant_seq=G;Dbxref=dbSNP_129:rs53752543;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1508	1508	.	+	.	ID=2860;Variant_seq=A;Dbxref=dbSNP_129:rs53920624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046014.1	dbSNP	SNV	1508	1508	.	+	.	ID=2861;Variant_seq=T;Dbxref=dbSNP_129:rs53092057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	insertion	1516	1516	.	+	.	ID=2862;Variant_seq=A;Dbxref=dbSNP_129:rs53722243;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	SNV	1524	1524	.	+	.	ID=2863;Variant_seq=T;Dbxref=dbSNP_129:rs53165287;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046014.1	dbSNP	SNV	1531	1531	.	+	.	ID=2864;Variant_seq=C;Dbxref=dbSNP_129:rs54321624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046014.1	dbSNP	SNV	1532	1532	.	+	.	ID=2865;Variant_seq=T;Dbxref=dbSNP_129:rs53015047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	deletion	1538	1545	.	+	.	ID=2866;Variant_seq=-;Dbxref=dbSNP_129:rs53025522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TTCTGGAC
AAAA02046014.1	dbSNP	SNV	1541	1541	.	+	.	ID=2867;Variant_seq=G;Dbxref=dbSNP_129:rs54239559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046014.1	dbSNP	insertion	1554	1554	.	+	.	ID=2868;Variant_seq=T;Dbxref=dbSNP_129:rs53374195;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1557	1557	.	+	.	ID=2869;Variant_seq=T;Dbxref=dbSNP_129:rs54006639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1558	1558	.	+	.	ID=2870;Variant_seq=G;Dbxref=dbSNP_129:rs53662747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1559	1559	.	+	.	ID=2871;Variant_seq=AAAGTC;Dbxref=dbSNP_129:rs53270451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1561	1561	.	+	.	ID=2872;Variant_seq=TCGTATTCCA;Dbxref=dbSNP_129:rs53327923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1565	1565	.	+	.	ID=2873;Variant_seq=CCA;Dbxref=dbSNP_129:rs52987770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	insertion	1571	1571	.	+	.	ID=2874;Variant_seq=TATAAATTC;Dbxref=dbSNP_129:rs54351165;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02046014.1	dbSNP	SNV	1584	1584	.	+	.	ID=2875;Variant_seq=T;Dbxref=dbSNP_129:rs53622623;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048285.1	dbSNP	SNV	1385	1385	.	+	.	ID=2876;Variant_seq=A;Dbxref=dbSNP_129:rs52965991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043719.1	dbSNP	SNV	1830	1830	.	+	.	ID=2877;Variant_seq=T;Dbxref=dbSNP_129:rs20283408;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043719.1	dbSNP	SNV	2113	2113	.	+	.	ID=2878;Variant_seq=C;Dbxref=dbSNP_129:rs19401145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043719.1	dbSNP	SNV	2124	2124	.	+	.	ID=2879;Variant_seq=C;Dbxref=dbSNP_129:rs19851322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043719.1	dbSNP	SNV	2136	2136	.	+	.	ID=2880;Variant_seq=G;Dbxref=dbSNP_129:rs19851332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037874.1	dbSNP	SNV	518	518	.	+	.	ID=2881;Variant_seq=T;Dbxref=dbSNP_129:rs53314900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037874.1	dbSNP	SNV	519	519	.	+	.	ID=2882;Variant_seq=G;Dbxref=dbSNP_129:rs53500036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037874.1	dbSNP	SNV	525	525	.	+	.	ID=2883;Variant_seq=C;Dbxref=dbSNP_129:rs54014608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037874.1	dbSNP	SNV	6631	6631	.	+	.	ID=2884;Variant_seq=T;Dbxref=dbSNP_129:rs53477259;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037874.1	dbSNP	SNV	7083	7083	.	+	.	ID=2885;Variant_seq=A;Dbxref=dbSNP_129:rs53477396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037874.1	dbSNP	SNV	7092	7092	.	+	.	ID=2886;Variant_seq=A;Dbxref=dbSNP_129:rs54165066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047340.1	dbSNP	SNV	257	257	.	+	.	ID=2887;Variant_seq=G;Dbxref=dbSNP_129:rs19475056;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047340.1	dbSNP	SNV	493	493	.	+	.	ID=2888;Variant_seq=T;Dbxref=dbSNP_129:rs19475046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047340.1	dbSNP	SNV	1828	1828	.	+	.	ID=2889;Variant_seq=T;Dbxref=dbSNP_129:rs19475026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047340.1	dbSNP	SNV	2434	2434	.	+	.	ID=2890;Variant_seq=C;Dbxref=dbSNP_129:rs19605749;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037940.1	dbSNP	SNV	5591	5591	.	+	.	ID=2891;Variant_seq=G;Dbxref=dbSNP_129:rs54392399;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037940.1	dbSNP	SNV	5593	5593	.	+	.	ID=2892;Variant_seq=T;Dbxref=dbSNP_129:rs54137364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037940.1	dbSNP	SNV	5594	5594	.	+	.	ID=2893;Variant_seq=T;Dbxref=dbSNP_129:rs53094607;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037940.1	dbSNP	SNV	5596	5596	.	+	.	ID=2894;Variant_seq=T;Dbxref=dbSNP_129:rs54095592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037940.1	dbSNP	SNV	8268	8268	.	+	.	ID=2895;Variant_seq=A;Dbxref=dbSNP_129:rs21354107;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02041448.1	dbSNP	SNV	454	454	.	+	.	ID=2896;Variant_seq=G;Dbxref=dbSNP_129:rs18262617;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041448.1	dbSNP	SNV	490	490	.	+	.	ID=2897;Variant_seq=C;Dbxref=dbSNP_129:rs18262581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041448.1	dbSNP	SNV	784	784	.	+	.	ID=2898;Variant_seq=T;Dbxref=dbSNP_129:rs17892701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041448.1	dbSNP	SNV	794	794	.	+	.	ID=2899;Variant_seq=A;Dbxref=dbSNP_129:rs18262347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041448.1	dbSNP	SNV	795	795	.	+	.	ID=2900;Variant_seq=T,C,G;Dbxref=dbSNP_129:rs17892702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041448.1	dbSNP	SNV	796	796	.	+	.	ID=2901;Variant_seq=G;Dbxref=dbSNP_129:rs18262338;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041448.1	dbSNP	SNV	800	800	.	+	.	ID=2902;Variant_seq=C;Dbxref=dbSNP_129:rs18262329;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02041448.1	dbSNP	SNV	839	839	.	+	.	ID=2903;Variant_seq=G;Dbxref=dbSNP_129:rs18262293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02041448.1	dbSNP	SNV	1252	1252	.	+	.	ID=2904;Variant_seq=G;Dbxref=dbSNP_129:rs18262176;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398852.1	dbSNP	SNV	706	706	.	+	.	ID=2905;Variant_seq=A;Dbxref=dbSNP_129:rs53775831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	2748	2748	.	+	.	ID=2906;Variant_seq=G;Dbxref=dbSNP_129:rs19110330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398852.1	dbSNP	SNV	3692	3692	.	+	.	ID=2907;Variant_seq=G;Dbxref=dbSNP_129:rs18990768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398852.1	dbSNP	SNV	4045	4045	.	+	.	ID=2908;Variant_seq=A;Dbxref=dbSNP_129:rs18992507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4046	4046	.	+	.	ID=2909;Variant_seq=G;Dbxref=dbSNP_129:rs18992517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4047	4047	.	+	.	ID=2910;Variant_seq=A;Dbxref=dbSNP_129:rs18992527;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4048	4048	.	+	.	ID=2911;Variant_seq=T;Dbxref=dbSNP_129:rs18992537;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4049	4049	.	+	.	ID=2912;Variant_seq=C;Dbxref=dbSNP_129:rs18992547;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4179	4179	.	+	.	ID=2913;Variant_seq=T;Dbxref=dbSNP_129:rs18993197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4180	4180	.	+	.	ID=2914;Variant_seq=T;Dbxref=dbSNP_129:rs18993207;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4182	4182	.	+	.	ID=2915;Variant_seq=T;Dbxref=dbSNP_129:rs18993217;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4183	4183	.	+	.	ID=2916;Variant_seq=T;Dbxref=dbSNP_129:rs18993227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4193	4193	.	+	.	ID=2917;Variant_seq=C;Dbxref=dbSNP_129:rs18993287;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4209	4209	.	+	.	ID=2918;Variant_seq=T;Dbxref=dbSNP_129:rs18993347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4256	4256	.	+	.	ID=2919;Variant_seq=C;Dbxref=dbSNP_129:rs18993497;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398852.1	dbSNP	SNV	4272	4272	.	+	.	ID=2920;Variant_seq=G;Dbxref=dbSNP_129:rs18993577;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398852.1	dbSNP	SNV	4275	4275	.	+	.	ID=2921;Variant_seq=T;Dbxref=dbSNP_129:rs18993587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4279	4279	.	+	.	ID=2922;Variant_seq=A;Dbxref=dbSNP_129:rs18993607;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4280	4280	.	+	.	ID=2923;Variant_seq=A;Dbxref=dbSNP_129:rs18993617;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398852.1	dbSNP	SNV	4282	4282	.	+	.	ID=2924;Variant_seq=T;Dbxref=dbSNP_129:rs18993627;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398852.1	dbSNP	SNV	4519	4519	.	+	.	ID=2925;Variant_seq=A;Dbxref=dbSNP_129:rs52872853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398860.1	dbSNP	SNV	1634	1634	.	+	.	ID=2926;Variant_seq=A;Dbxref=dbSNP_129:rs53210535;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398860.1	dbSNP	deletion	1667	1672	.	+	.	ID=2927;Variant_seq=-;Dbxref=dbSNP_129:rs53234973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TGATCG
CH398860.1	dbSNP	SNV	1946	1946	.	+	.	ID=2928;Variant_seq=A;Dbxref=dbSNP_129:rs20868150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398860.1	dbSNP	SNV	2208	2208	.	+	.	ID=2929;Variant_seq=A;Dbxref=dbSNP_129:rs20922469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398860.1	dbSNP	SNV	2252	2252	.	+	.	ID=2930;Variant_seq=T;Dbxref=dbSNP_129:rs20061947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398860.1	dbSNP	SNV	2289	2289	.	+	.	ID=2931;Variant_seq=A;Dbxref=dbSNP_129:rs20061937;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398860.1	dbSNP	SNV	2855	2855	.	+	.	ID=2932;Variant_seq=T;Dbxref=dbSNP_129:rs21583017;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398860.1	dbSNP	SNV	2880	2880	.	+	.	ID=2933;Variant_seq=T;Dbxref=dbSNP_129:rs53437768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398860.1	dbSNP	SNV	2928	2928	.	+	.	ID=2934;Variant_seq=A;Dbxref=dbSNP_129:rs21231272;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047850.1	dbSNP	SNV	177	177	.	+	.	ID=2935;Variant_seq=C;Dbxref=dbSNP_129:rs21322133;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02047850.1	dbSNP	SNV	339	339	.	+	.	ID=2936;Variant_seq=A;Dbxref=dbSNP_129:rs21322153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047850.1	dbSNP	SNV	816	816	.	+	.	ID=2937;Variant_seq=A;Dbxref=dbSNP_129:rs54225240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399337.1	dbSNP	SNV	3684	3684	.	+	.	ID=2938;Variant_seq=T;Dbxref=dbSNP_129:rs21365245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4536	4536	.	+	.	ID=2939;Variant_seq=T;Dbxref=dbSNP_129:rs21362303;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4837	4837	.	+	.	ID=2940;Variant_seq=G;Dbxref=dbSNP_129:rs21361193;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4838	4838	.	+	.	ID=2941;Variant_seq=G;Dbxref=dbSNP_129:rs21361183;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4839	4839	.	+	.	ID=2942;Variant_seq=T;Dbxref=dbSNP_129:rs21361173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4841	4841	.	+	.	ID=2943;Variant_seq=A;Dbxref=dbSNP_129:rs21361163;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4844	4844	.	+	.	ID=2944;Variant_seq=G;Dbxref=dbSNP_129:rs21361143;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399337.1	dbSNP	SNV	4849	4849	.	+	.	ID=2945;Variant_seq=G;Dbxref=dbSNP_129:rs21361113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4850	4850	.	+	.	ID=2946;Variant_seq=G;Dbxref=dbSNP_129:rs21361103;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399337.1	dbSNP	SNV	4852	4852	.	+	.	ID=2947;Variant_seq=A;Dbxref=dbSNP_129:rs21361093;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4853	4853	.	+	.	ID=2948;Variant_seq=G;Dbxref=dbSNP_129:rs21361083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399337.1	dbSNP	SNV	4857	4857	.	+	.	ID=2949;Variant_seq=T;Dbxref=dbSNP_129:rs21361063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4862	4862	.	+	.	ID=2950;Variant_seq=G;Dbxref=dbSNP_129:rs21361053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399337.1	dbSNP	SNV	4869	4869	.	+	.	ID=2951;Variant_seq=G;Dbxref=dbSNP_129:rs21361043;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399337.1	dbSNP	SNV	4874	4874	.	+	.	ID=2952;Variant_seq=G;Dbxref=dbSNP_129:rs21361033;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4886	4886	.	+	.	ID=2953;Variant_seq=C;Dbxref=dbSNP_129:rs21361013;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399337.1	dbSNP	SNV	4898	4898	.	+	.	ID=2954;Variant_seq=A;Dbxref=dbSNP_129:rs21360983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4904	4904	.	+	.	ID=2955;Variant_seq=G;Dbxref=dbSNP_129:rs21360963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399337.1	dbSNP	SNV	4905	4905	.	+	.	ID=2956;Variant_seq=G;Dbxref=dbSNP_129:rs21360953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	257	257	.	+	.	ID=2957;Variant_seq=T;Dbxref=dbSNP_129:rs53791524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	667	667	.	+	.	ID=2958;Variant_seq=G;Dbxref=dbSNP_129:rs53327030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	678	678	.	+	.	ID=2959;Variant_seq=A;Dbxref=dbSNP_129:rs52874559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	679	679	.	+	.	ID=2960;Variant_seq=A;Dbxref=dbSNP_129:rs54370506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	719	719	.	+	.	ID=2961;Variant_seq=A;Dbxref=dbSNP_129:rs53308570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	753	753	.	+	.	ID=2962;Variant_seq=A;Dbxref=dbSNP_129:rs53194203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	761	761	.	+	.	ID=2963;Variant_seq=A;Dbxref=dbSNP_129:rs53733978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	766	766	.	+	.	ID=2964;Variant_seq=G;Dbxref=dbSNP_129:rs53130313;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	767	767	.	+	.	ID=2965;Variant_seq=A;Dbxref=dbSNP_129:rs53000282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	1427	1427	.	+	.	ID=2966;Variant_seq=T;Dbxref=dbSNP_129:rs18819721;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	1435	1435	.	+	.	ID=2967;Variant_seq=T;Dbxref=dbSNP_129:rs18819701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	1547	1547	.	+	.	ID=2968;Variant_seq=G;Dbxref=dbSNP_129:rs18819621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	1548	1548	.	+	.	ID=2969;Variant_seq=T;Dbxref=dbSNP_129:rs18819611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	1552	1552	.	+	.	ID=2970;Variant_seq=G;Dbxref=dbSNP_129:rs18819601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037585.1	dbSNP	SNV	1575	1575	.	+	.	ID=2971;Variant_seq=A;Dbxref=dbSNP_129:rs18819571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	1576	1576	.	+	.	ID=2972;Variant_seq=A;Dbxref=dbSNP_129:rs18819561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	1598	1598	.	+	.	ID=2973;Variant_seq=G;Dbxref=dbSNP_129:rs18819531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	1667	1667	.	+	.	ID=2974;Variant_seq=C;Dbxref=dbSNP_129:rs21132421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037585.1	dbSNP	SNV	1799	1799	.	+	.	ID=2975;Variant_seq=A,T,G;Dbxref=dbSNP_129:rs17887434;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	1808	1808	.	+	.	ID=2976;Variant_seq=A;Dbxref=dbSNP_129:rs18819282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	1822	1822	.	+	.	ID=2977;Variant_seq=G;Dbxref=dbSNP_129:rs18819262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	1857	1857	.	+	.	ID=2978;Variant_seq=A;Dbxref=dbSNP_129:rs18819232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	2219	2219	.	+	.	ID=2979;Variant_seq=A;Dbxref=dbSNP_129:rs18819342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	2224	2224	.	+	.	ID=2980;Variant_seq=A;Dbxref=dbSNP_129:rs18819332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	2241	2241	.	+	.	ID=2981;Variant_seq=G;Dbxref=dbSNP_129:rs18819322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	2259	2259	.	+	.	ID=2982;Variant_seq=A;Dbxref=dbSNP_129:rs18819312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	2339	2339	.	+	.	ID=2983;Variant_seq=A;Dbxref=dbSNP_129:rs18818649;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037585.1	dbSNP	SNV	2362	2362	.	+	.	ID=2984;Variant_seq=G;Dbxref=dbSNP_129:rs18818619;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	2487	2487	.	+	.	ID=2985;Variant_seq=T;Dbxref=dbSNP_129:rs18818509;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	2491	2491	.	+	.	ID=2986;Variant_seq=T;Dbxref=dbSNP_129:rs18818499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	2493	2493	.	+	.	ID=2987;Variant_seq=G;Dbxref=dbSNP_129:rs18818489;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	2500	2500	.	+	.	ID=2988;Variant_seq=T;Dbxref=dbSNP_129:rs18818479;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037585.1	dbSNP	SNV	2501	2501	.	+	.	ID=2989;Variant_seq=T;Dbxref=dbSNP_129:rs18818469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037585.1	dbSNP	SNV	4166	4166	.	+	.	ID=2990;Variant_seq=T;Dbxref=dbSNP_129:rs53406587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037585.1	dbSNP	SNV	9621	9621	.	+	.	ID=2991;Variant_seq=T;Dbxref=dbSNP_129:rs54045369;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	1091	1091	.	+	.	ID=2992;Variant_seq=C;Dbxref=dbSNP_129:rs19051222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	1133	1133	.	+	.	ID=2993;Variant_seq=G;Dbxref=dbSNP_129:rs19051252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	1368	1368	.	+	.	ID=2994;Variant_seq=T;Dbxref=dbSNP_129:rs19051427;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	1731	1731	.	+	.	ID=2995;Variant_seq=G;Dbxref=dbSNP_129:rs19051798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	1739	1739	.	+	.	ID=2996;Variant_seq=T;Dbxref=dbSNP_129:rs19051808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	1742	1742	.	+	.	ID=2997;Variant_seq=G;Dbxref=dbSNP_129:rs19051818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	1744	1744	.	+	.	ID=2998;Variant_seq=G;Dbxref=dbSNP_129:rs19051828;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399292.1	dbSNP	SNV	1913	1913	.	+	.	ID=2999;Variant_seq=G;Dbxref=dbSNP_129:rs19051967;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	1949	1949	.	+	.	ID=3000;Variant_seq=A;Dbxref=dbSNP_129:rs19051987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	1995	1995	.	+	.	ID=3001;Variant_seq=A;Dbxref=dbSNP_129:rs19051997;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2074	2074	.	+	.	ID=3002;Variant_seq=T;Dbxref=dbSNP_129:rs19052069;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	2650	2650	.	+	.	ID=3003;Variant_seq=A;Dbxref=dbSNP_129:rs54101861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2678	2678	.	+	.	ID=3004;Variant_seq=T;Dbxref=dbSNP_129:rs19052593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	2735	2735	.	+	.	ID=3005;Variant_seq=A;Dbxref=dbSNP_129:rs19052654;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2737	2737	.	+	.	ID=3006;Variant_seq=G;Dbxref=dbSNP_129:rs19052664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	2863	2863	.	+	.	ID=3007;Variant_seq=T;Dbxref=dbSNP_129:rs19052725;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	2868	2868	.	+	.	ID=3008;Variant_seq=A;Dbxref=dbSNP_129:rs19052735;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2871	2871	.	+	.	ID=3009;Variant_seq=T;Dbxref=dbSNP_129:rs19052745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399292.1	dbSNP	SNV	2881	2881	.	+	.	ID=3010;Variant_seq=C;Dbxref=dbSNP_129:rs19052765;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	2885	2885	.	+	.	ID=3011;Variant_seq=C;Dbxref=dbSNP_129:rs19052775;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399292.1	dbSNP	SNV	2894	2894	.	+	.	ID=3012;Variant_seq=A;Dbxref=dbSNP_129:rs19052805;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2915	2915	.	+	.	ID=3013;Variant_seq=T;Dbxref=dbSNP_129:rs19052835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	2928	2928	.	+	.	ID=3014;Variant_seq=A;Dbxref=dbSNP_129:rs19052845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2929	2929	.	+	.	ID=3015;Variant_seq=G;Dbxref=dbSNP_129:rs19052855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399292.1	dbSNP	SNV	2933	2933	.	+	.	ID=3016;Variant_seq=T;Dbxref=dbSNP_129:rs19052865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399292.1	dbSNP	SNV	2945	2945	.	+	.	ID=3017;Variant_seq=C;Dbxref=dbSNP_129:rs19052885;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399292.1	dbSNP	SNV	2951	2951	.	+	.	ID=3018;Variant_seq=G;Dbxref=dbSNP_129:rs19052905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399292.1	dbSNP	SNV	3113	3113	.	+	.	ID=3019;Variant_seq=C;Dbxref=dbSNP_129:rs19053047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399292.1	dbSNP	SNV	6059	6059	.	+	.	ID=3020;Variant_seq=C;Dbxref=dbSNP_129:rs21756231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046072.1	dbSNP	SNV	385	385	.	+	.	ID=3021;Variant_seq=C;Dbxref=dbSNP_129:rs19106001;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH401049.1	dbSNP	SNV	1319	1319	.	+	.	ID=3022;Variant_seq=A;Dbxref=dbSNP_129:rs53326957;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH401049.1	dbSNP	SNV	1320	1320	.	+	.	ID=3023;Variant_seq=C;Dbxref=dbSNP_129:rs53379936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH401049.1	dbSNP	SNV	1321	1321	.	+	.	ID=3024;Variant_seq=C;Dbxref=dbSNP_129:rs54186947;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH401049.1	dbSNP	SNV	1322	1322	.	+	.	ID=3025;Variant_seq=T;Dbxref=dbSNP_129:rs53682663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401049.1	dbSNP	SNV	1323	1323	.	+	.	ID=3026;Variant_seq=G;Dbxref=dbSNP_129:rs54366818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401049.1	dbSNP	SNV	1325	1325	.	+	.	ID=3027;Variant_seq=A;Dbxref=dbSNP_129:rs52937284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401049.1	dbSNP	SNV	1326	1326	.	+	.	ID=3028;Variant_seq=A;Dbxref=dbSNP_129:rs53685494;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401049.1	dbSNP	SNV	1330	1330	.	+	.	ID=3029;Variant_seq=T,G;Dbxref=dbSNP_129:rs53178111;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045867.1	dbSNP	SNV	2388	2388	.	+	.	ID=3030;Variant_seq=C;Dbxref=dbSNP_129:rs19186640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045867.1	dbSNP	SNV	2471	2471	.	+	.	ID=3031;Variant_seq=G;Dbxref=dbSNP_129:rs19186650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045867.1	dbSNP	SNV	2494	2494	.	+	.	ID=3032;Variant_seq=C;Dbxref=dbSNP_129:rs19186660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045867.1	dbSNP	SNV	2776	2776	.	+	.	ID=3033;Variant_seq=T;Dbxref=dbSNP_129:rs19186680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045867.1	dbSNP	SNV	2785	2785	.	+	.	ID=3034;Variant_seq=C;Dbxref=dbSNP_129:rs19186690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044635.1	dbSNP	SNV	1315	1315	.	+	.	ID=3035;Variant_seq=A;Dbxref=dbSNP_129:rs21067601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044635.1	dbSNP	SNV	1318	1318	.	+	.	ID=3036;Variant_seq=T;Dbxref=dbSNP_129:rs21067611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044635.1	dbSNP	SNV	1327	1327	.	+	.	ID=3037;Variant_seq=T;Dbxref=dbSNP_129:rs21067621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044635.1	dbSNP	SNV	3002	3002	.	+	.	ID=3038;Variant_seq=G;Dbxref=dbSNP_129:rs21070941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044635.1	dbSNP	SNV	3110	3110	.	+	.	ID=3039;Variant_seq=C;Dbxref=dbSNP_129:rs21071161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049300.1	dbSNP	SNV	754	754	.	+	.	ID=3040;Variant_seq=A;Dbxref=dbSNP_129:rs54411066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049300.1	dbSNP	insertion	760	760	.	+	.	ID=3041;Variant_seq=A;Dbxref=dbSNP_129:rs53317270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02049300.1	dbSNP	SNV	763	763	.	+	.	ID=3042;Variant_seq=T;Dbxref=dbSNP_129:rs53423237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049300.1	dbSNP	SNV	776	776	.	+	.	ID=3043;Variant_seq=T;Dbxref=dbSNP_129:rs54253869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049300.1	dbSNP	SNV	785	785	.	+	.	ID=3044;Variant_seq=A;Dbxref=dbSNP_129:rs53825674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049300.1	dbSNP	SNV	787	787	.	+	.	ID=3045;Variant_seq=A;Dbxref=dbSNP_129:rs53278865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049300.1	dbSNP	SNV	789	789	.	+	.	ID=3046;Variant_seq=A;Dbxref=dbSNP_129:rs54072499;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02049300.1	dbSNP	deletion	792	792	.	+	.	ID=3047;Variant_seq=-;Dbxref=dbSNP_129:rs54072992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049300.1	dbSNP	SNV	806	806	.	+	.	ID=3048;Variant_seq=T;Dbxref=dbSNP_129:rs53327363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049300.1	dbSNP	SNV	807	807	.	+	.	ID=3049;Variant_seq=A;Dbxref=dbSNP_129:rs54368481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02049300.1	dbSNP	SNV	815	815	.	+	.	ID=3050;Variant_seq=A;Dbxref=dbSNP_129:rs53441587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047262.1	dbSNP	SNV	2224	2224	.	+	.	ID=3051;Variant_seq=A;Dbxref=dbSNP_129:rs54161435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047262.1	dbSNP	SNV	2229	2229	.	+	.	ID=3052;Variant_seq=G;Dbxref=dbSNP_129:rs52996132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047262.1	dbSNP	SNV	2235	2235	.	+	.	ID=3053;Variant_seq=A;Dbxref=dbSNP_129:rs53433233;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035589.1	dbSNP	SNV	2184	2184	.	+	.	ID=3054;Variant_seq=T;Dbxref=dbSNP_129:rs21466789;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035589.1	dbSNP	SNV	2220	2220	.	+	.	ID=3055;Variant_seq=T;Dbxref=dbSNP_129:rs21111224;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035589.1	dbSNP	SNV	19933	19933	.	+	.	ID=3056;Variant_seq=C;Dbxref=dbSNP_129:rs54016014;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035589.1	dbSNP	SNV	20218	20218	.	+	.	ID=3057;Variant_seq=A;Dbxref=dbSNP_129:rs53819440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040360.1	dbSNP	SNV	1743	1743	.	+	.	ID=3058;Variant_seq=C;Dbxref=dbSNP_129:rs20684895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040360.1	dbSNP	SNV	2873	2873	.	+	.	ID=3059;Variant_seq=T;Dbxref=dbSNP_129:rs19046019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040360.1	dbSNP	SNV	3351	3351	.	+	.	ID=3060;Variant_seq=C;Dbxref=dbSNP_129:rs19092677;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040360.1	dbSNP	SNV	4025	4025	.	+	.	ID=3061;Variant_seq=G;Dbxref=dbSNP_129:rs19734220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040360.1	dbSNP	SNV	4861	4861	.	+	.	ID=3062;Variant_seq=G;Dbxref=dbSNP_129:rs53997861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040360.1	dbSNP	SNV	4862	4862	.	+	.	ID=3063;Variant_seq=C;Dbxref=dbSNP_129:rs53708197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398887.1	dbSNP	SNV	1633	1633	.	+	.	ID=3064;Variant_seq=T;Dbxref=dbSNP_129:rs20297599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398887.1	dbSNP	SNV	1705	1705	.	+	.	ID=3065;Variant_seq=C;Dbxref=dbSNP_129:rs20301190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398887.1	dbSNP	SNV	1724	1724	.	+	.	ID=3066;Variant_seq=C;Dbxref=dbSNP_129:rs20301210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398887.1	dbSNP	SNV	2577	2577	.	+	.	ID=3067;Variant_seq=A;Dbxref=dbSNP_129:rs20297729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398887.1	dbSNP	SNV	4250	4250	.	+	.	ID=3068;Variant_seq=G;Dbxref=dbSNP_129:rs20298541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398887.1	dbSNP	SNV	5555	5555	.	+	.	ID=3069;Variant_seq=T;Dbxref=dbSNP_129:rs20298841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398887.1	dbSNP	SNV	6117	6117	.	+	.	ID=3070;Variant_seq=T;Dbxref=dbSNP_129:rs20297124;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044967.1	dbSNP	SNV	2894	2894	.	+	.	ID=3071;Variant_seq=A;Dbxref=dbSNP_129:rs20887979;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044967.1	dbSNP	SNV	2907	2907	.	+	.	ID=3072;Variant_seq=T;Dbxref=dbSNP_129:rs20887989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044967.1	dbSNP	SNV	2963	2963	.	+	.	ID=3073;Variant_seq=G;Dbxref=dbSNP_129:rs20888019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050079.1	dbSNP	SNV	1061	1061	.	+	.	ID=3074;Variant_seq=A;Dbxref=dbSNP_129:rs19946948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	1840	1840	.	+	.	ID=3075;Variant_seq=T;Dbxref=dbSNP_129:rs19656673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399404.1	dbSNP	SNV	1909	1909	.	+	.	ID=3076;Variant_seq=C;Dbxref=dbSNP_129:rs19656683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	2462	2462	.	+	.	ID=3077;Variant_seq=C;Dbxref=dbSNP_129:rs18875248;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	2470	2470	.	+	.	ID=3078;Variant_seq=C;Dbxref=dbSNP_129:rs18875238;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	2471	2471	.	+	.	ID=3079;Variant_seq=G;Dbxref=dbSNP_129:rs18875228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399404.1	dbSNP	SNV	3014	3014	.	+	.	ID=3080;Variant_seq=A;Dbxref=dbSNP_129:rs53916371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	3053	3053	.	+	.	ID=3081;Variant_seq=C;Dbxref=dbSNP_129:rs20079130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	3053	3053	.	+	.	ID=3082;Variant_seq=A;Dbxref=dbSNP_129:rs53017651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	3057	3057	.	+	.	ID=3083;Variant_seq=C;Dbxref=dbSNP_129:rs20079150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399404.1	dbSNP	SNV	3064	3064	.	+	.	ID=3084;Variant_seq=T;Dbxref=dbSNP_129:rs53580693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399404.1	dbSNP	SNV	3073	3073	.	+	.	ID=3085;Variant_seq=T;Dbxref=dbSNP_129:rs53388305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399404.1	dbSNP	SNV	3737	3737	.	+	.	ID=3086;Variant_seq=A;Dbxref=dbSNP_129:rs53324344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399550.1	dbSNP	SNV	1065	1065	.	+	.	ID=3087;Variant_seq=C;Dbxref=dbSNP_129:rs18861571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046035.1	dbSNP	SNV	677	677	.	+	.	ID=3088;Variant_seq=A;Dbxref=dbSNP_129:rs21141404;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046035.1	dbSNP	SNV	806	806	.	+	.	ID=3089;Variant_seq=A;Dbxref=dbSNP_129:rs21141384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046035.1	dbSNP	SNV	2175	2175	.	+	.	ID=3090;Variant_seq=T;Dbxref=dbSNP_129:rs17955077;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048042.1	dbSNP	SNV	1741	1741	.	+	.	ID=3091;Variant_seq=G;Dbxref=dbSNP_129:rs20304369;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046563.1	dbSNP	SNV	395	395	.	+	.	ID=3092;Variant_seq=C;Dbxref=dbSNP_129:rs19882417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046563.1	dbSNP	SNV	407	407	.	+	.	ID=3093;Variant_seq=C;Dbxref=dbSNP_129:rs19882377;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1485	1485	.	+	.	ID=3094;Variant_seq=T;Dbxref=dbSNP_129:rs53382542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1486	1486	.	+	.	ID=3095;Variant_seq=G;Dbxref=dbSNP_129:rs53599632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1486	1486	.	+	.	ID=3096;Variant_seq=G;Dbxref=dbSNP_129:rs52912835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1501	1501	.	+	.	ID=3097;Variant_seq=C;Dbxref=dbSNP_129:rs53043412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044701.1	dbSNP	SNV	1505	1505	.	+	.	ID=3098;Variant_seq=T;Dbxref=dbSNP_129:rs53908371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1507	1507	.	+	.	ID=3099;Variant_seq=G;Dbxref=dbSNP_129:rs54362346;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	1533	1533	.	+	.	ID=3100;Variant_seq=T;Dbxref=dbSNP_129:rs52964115;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044701.1	dbSNP	SNV	1534	1534	.	+	.	ID=3101;Variant_seq=A;Dbxref=dbSNP_129:rs53916534;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	1535	1535	.	+	.	ID=3102;Variant_seq=A;Dbxref=dbSNP_129:rs52981916;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	1543	1543	.	+	.	ID=3103;Variant_seq=A;Dbxref=dbSNP_129:rs53952225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	2167	2167	.	+	.	ID=3104;Variant_seq=A;Dbxref=dbSNP_129:rs52935668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	2185	2185	.	+	.	ID=3105;Variant_seq=A;Dbxref=dbSNP_129:rs53956710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	2272	2272	.	+	.	ID=3106;Variant_seq=A;Dbxref=dbSNP_129:rs20614744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	2273	2273	.	+	.	ID=3107;Variant_seq=G;Dbxref=dbSNP_129:rs20614734;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044701.1	dbSNP	SNV	2278	2278	.	+	.	ID=3108;Variant_seq=C;Dbxref=dbSNP_129:rs20614714;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044701.1	dbSNP	SNV	2281	2281	.	+	.	ID=3109;Variant_seq=A;Dbxref=dbSNP_129:rs20614704;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044701.1	dbSNP	SNV	2290	2290	.	+	.	ID=3110;Variant_seq=C;Dbxref=dbSNP_129:rs20614674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044701.1	dbSNP	SNV	2296	2296	.	+	.	ID=3111;Variant_seq=C;Dbxref=dbSNP_129:rs20614664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048471.1	dbSNP	SNV	240	240	.	+	.	ID=3112;Variant_seq=G;Dbxref=dbSNP_129:rs19691717;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048471.1	dbSNP	SNV	241	241	.	+	.	ID=3113;Variant_seq=A;Dbxref=dbSNP_129:rs19691727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048471.1	dbSNP	SNV	248	248	.	+	.	ID=3114;Variant_seq=C;Dbxref=dbSNP_129:rs19691737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048471.1	dbSNP	SNV	249	249	.	+	.	ID=3115;Variant_seq=G;Dbxref=dbSNP_129:rs19691747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048471.1	dbSNP	SNV	253	253	.	+	.	ID=3116;Variant_seq=A;Dbxref=dbSNP_129:rs19691757;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048471.1	dbSNP	SNV	256	256	.	+	.	ID=3117;Variant_seq=T;Dbxref=dbSNP_129:rs19691767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048471.1	dbSNP	SNV	260	260	.	+	.	ID=3118;Variant_seq=T;Dbxref=dbSNP_129:rs19691787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048471.1	dbSNP	SNV	265	265	.	+	.	ID=3119;Variant_seq=T;Dbxref=dbSNP_129:rs19691807;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048471.1	dbSNP	SNV	272	272	.	+	.	ID=3120;Variant_seq=C;Dbxref=dbSNP_129:rs19691817;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048471.1	dbSNP	SNV	274	274	.	+	.	ID=3121;Variant_seq=T;Dbxref=dbSNP_129:rs19691827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048471.1	dbSNP	SNV	286	286	.	+	.	ID=3122;Variant_seq=G;Dbxref=dbSNP_129:rs19691837;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048471.1	dbSNP	SNV	1198	1198	.	+	.	ID=3123;Variant_seq=T;Dbxref=dbSNP_129:rs19693647;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02048471.1	dbSNP	SNV	1199	1199	.	+	.	ID=3124;Variant_seq=G;Dbxref=dbSNP_129:rs19693657;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045545.1	dbSNP	SNV	267	267	.	+	.	ID=3125;Variant_seq=T;Dbxref=dbSNP_129:rs54386302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045545.1	dbSNP	SNV	269	269	.	+	.	ID=3126;Variant_seq=A;Dbxref=dbSNP_129:rs53865051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045545.1	dbSNP	SNV	452	452	.	+	.	ID=3127;Variant_seq=C;Dbxref=dbSNP_129:rs20168249;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045545.1	dbSNP	SNV	1097	1097	.	+	.	ID=3128;Variant_seq=T;Dbxref=dbSNP_129:rs20295725;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045545.1	dbSNP	SNV	1174	1174	.	+	.	ID=3129;Variant_seq=C;Dbxref=dbSNP_129:rs52841640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045545.1	dbSNP	SNV	2699	2699	.	+	.	ID=3130;Variant_seq=G;Dbxref=dbSNP_129:rs20445788;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045545.1	dbSNP	SNV	2718	2718	.	+	.	ID=3131;Variant_seq=T;Dbxref=dbSNP_129:rs20445778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045545.1	dbSNP	SNV	2748	2748	.	+	.	ID=3132;Variant_seq=G;Dbxref=dbSNP_129:rs53963432;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045545.1	dbSNP	SNV	2763	2763	.	+	.	ID=3133;Variant_seq=A;Dbxref=dbSNP_129:rs54331741;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045545.1	dbSNP	SNV	2766	2766	.	+	.	ID=3134;Variant_seq=G;Dbxref=dbSNP_129:rs54013804;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045545.1	dbSNP	SNV	2770	2770	.	+	.	ID=3135;Variant_seq=G;Dbxref=dbSNP_129:rs53462734;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045545.1	dbSNP	SNV	2830	2830	.	+	.	ID=3136;Variant_seq=A;Dbxref=dbSNP_129:rs20445758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042135.1	dbSNP	insertion	1353	1353	.	+	.	ID=3137;Variant_seq=A;Dbxref=dbSNP_129:rs53290477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02042135.1	dbSNP	SNV	1357	1357	.	+	.	ID=3138;Variant_seq=A;Dbxref=dbSNP_129:rs52897838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042135.1	dbSNP	SNV	3203	3203	.	+	.	ID=3139;Variant_seq=C;Dbxref=dbSNP_129:rs19807808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02042135.1	dbSNP	SNV	3204	3204	.	+	.	ID=3140;Variant_seq=A;Dbxref=dbSNP_129:rs19807799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036498.1	dbSNP	SNV	712	712	.	+	.	ID=3141;Variant_seq=T;Dbxref=dbSNP_129:rs19674679;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	733	733	.	+	.	ID=3142;Variant_seq=T;Dbxref=dbSNP_129:rs53688830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	784	784	.	+	.	ID=3143;Variant_seq=A;Dbxref=dbSNP_129:rs19674639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036498.1	dbSNP	SNV	838	838	.	+	.	ID=3144;Variant_seq=A;Dbxref=dbSNP_129:rs20172175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036498.1	dbSNP	SNV	844	844	.	+	.	ID=3145;Variant_seq=G;Dbxref=dbSNP_129:rs20172185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036498.1	dbSNP	SNV	4822	4822	.	+	.	ID=3146;Variant_seq=C;Dbxref=dbSNP_129:rs19730507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036498.1	dbSNP	SNV	7849	7849	.	+	.	ID=3147;Variant_seq=T;Dbxref=dbSNP_129:rs54179900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	7851	7851	.	+	.	ID=3148;Variant_seq=A;Dbxref=dbSNP_129:rs53143251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036498.1	dbSNP	SNV	8061	8061	.	+	.	ID=3149;Variant_seq=T;Dbxref=dbSNP_129:rs54135819;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	8062	8062	.	+	.	ID=3150;Variant_seq=G;Dbxref=dbSNP_129:rs54402373;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	8071	8071	.	+	.	ID=3151;Variant_seq=T;Dbxref=dbSNP_129:rs54171642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	8073	8073	.	+	.	ID=3152;Variant_seq=A;Dbxref=dbSNP_129:rs54090330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02036498.1	dbSNP	SNV	8083	8083	.	+	.	ID=3153;Variant_seq=A;Dbxref=dbSNP_129:rs53031433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02036498.1	dbSNP	SNV	8084	8084	.	+	.	ID=3154;Variant_seq=T;Dbxref=dbSNP_129:rs54270744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02036498.1	dbSNP	SNV	12504	12504	.	+	.	ID=3155;Variant_seq=G;Dbxref=dbSNP_129:rs54156341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02036498.1	dbSNP	SNV	12508	12508	.	+	.	ID=3156;Variant_seq=A;Dbxref=dbSNP_129:rs53577691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399903.1	dbSNP	SNV	1880	1880	.	+	.	ID=3157;Variant_seq=T;Dbxref=dbSNP_129:rs53317384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399903.1	dbSNP	deletion	1888	1888	.	+	.	ID=3158;Variant_seq=-;Dbxref=dbSNP_129:rs54383248;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399903.1	dbSNP	SNV	1899	1899	.	+	.	ID=3159;Variant_seq=A;Dbxref=dbSNP_129:rs53767645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399903.1	dbSNP	deletion	1904	1904	.	+	.	ID=3160;Variant_seq=-;Dbxref=dbSNP_129:rs53163896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399903.1	dbSNP	deletion	3451	3451	.	+	.	ID=3161;Variant_seq=-;Dbxref=dbSNP_129:rs53163896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399903.1	dbSNP	SNV	3456	3456	.	+	.	ID=3162;Variant_seq=A;Dbxref=dbSNP_129:rs53767645;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399903.1	dbSNP	deletion	3467	3467	.	+	.	ID=3163;Variant_seq=-;Dbxref=dbSNP_129:rs54383248;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399903.1	dbSNP	SNV	3475	3475	.	+	.	ID=3164;Variant_seq=T;Dbxref=dbSNP_129:rs53317384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037017.1	dbSNP	SNV	581	581	.	+	.	ID=3165;Variant_seq=G;Dbxref=dbSNP_129:rs21256591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037017.1	dbSNP	SNV	696	696	.	+	.	ID=3166;Variant_seq=T;Dbxref=dbSNP_129:rs21256581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	705	705	.	+	.	ID=3167;Variant_seq=C;Dbxref=dbSNP_129:rs53665608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037017.1	dbSNP	SNV	757	757	.	+	.	ID=3168;Variant_seq=G;Dbxref=dbSNP_129:rs21256571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	818	818	.	+	.	ID=3169;Variant_seq=T;Dbxref=dbSNP_129:rs21256561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	954	954	.	+	.	ID=3170;Variant_seq=T;Dbxref=dbSNP_129:rs53062137;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037017.1	dbSNP	SNV	7500	7500	.	+	.	ID=3171;Variant_seq=T;Dbxref=dbSNP_129:rs52843802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037017.1	dbSNP	SNV	8617	8617	.	+	.	ID=3172;Variant_seq=T;Dbxref=dbSNP_129:rs19365105;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	8711	8711	.	+	.	ID=3173;Variant_seq=A;Dbxref=dbSNP_129:rs19973136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	9831	9831	.	+	.	ID=3174;Variant_seq=T;Dbxref=dbSNP_129:rs21125634;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	9832	9832	.	+	.	ID=3175;Variant_seq=G;Dbxref=dbSNP_129:rs21125644;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	9838	9838	.	+	.	ID=3176;Variant_seq=C;Dbxref=dbSNP_129:rs21125654;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	9839	9839	.	+	.	ID=3177;Variant_seq=A;Dbxref=dbSNP_129:rs21125664;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	9840	9840	.	+	.	ID=3178;Variant_seq=A;Dbxref=dbSNP_129:rs21125674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037017.1	dbSNP	SNV	11101	11101	.	+	.	ID=3179;Variant_seq=C;Dbxref=dbSNP_129:rs21125874;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	11102	11102	.	+	.	ID=3180;Variant_seq=G;Dbxref=dbSNP_129:rs21125884;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037017.1	dbSNP	SNV	11804	11804	.	+	.	ID=3181;Variant_seq=G;Dbxref=dbSNP_129:rs53254361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02042396.1	dbSNP	SNV	1037	1037	.	+	.	ID=3182;Variant_seq=T;Dbxref=dbSNP_129:rs53559759;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042396.1	dbSNP	SNV	1500	1500	.	+	.	ID=3183;Variant_seq=A;Dbxref=dbSNP_129:rs53230583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042396.1	dbSNP	SNV	1530	1530	.	+	.	ID=3184;Variant_seq=T;Dbxref=dbSNP_129:rs53257675;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	202	202	.	+	.	ID=3185;Variant_seq=G;Dbxref=dbSNP_129:rs18483898;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046961.1	dbSNP	SNV	203	203	.	+	.	ID=3186;Variant_seq=G;Dbxref=dbSNP_129:rs18483889;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046961.1	dbSNP	SNV	220	220	.	+	.	ID=3187;Variant_seq=G;Dbxref=dbSNP_129:rs20833888;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	309	309	.	+	.	ID=3188;Variant_seq=A;Dbxref=dbSNP_129:rs21358950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	405	405	.	+	.	ID=3189;Variant_seq=T;Dbxref=dbSNP_129:rs21358940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	589	589	.	+	.	ID=3190;Variant_seq=T;Dbxref=dbSNP_129:rs21358920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	671	671	.	+	.	ID=3191;Variant_seq=C;Dbxref=dbSNP_129:rs21358910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046961.1	dbSNP	SNV	861	861	.	+	.	ID=3192;Variant_seq=T;Dbxref=dbSNP_129:rs21358900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	997	997	.	+	.	ID=3193;Variant_seq=C;Dbxref=dbSNP_129:rs21358890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046961.1	dbSNP	SNV	1184	1184	.	+	.	ID=3194;Variant_seq=T;Dbxref=dbSNP_129:rs21552395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02046961.1	dbSNP	SNV	1309	1309	.	+	.	ID=3195;Variant_seq=C;Dbxref=dbSNP_129:rs21358870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046961.1	dbSNP	SNV	1742	1742	.	+	.	ID=3196;Variant_seq=A;Dbxref=dbSNP_129:rs21358850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046961.1	dbSNP	SNV	1923	1923	.	+	.	ID=3197;Variant_seq=G;Dbxref=dbSNP_129:rs21358840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046961.1	dbSNP	SNV	2135	2135	.	+	.	ID=3198;Variant_seq=T;Dbxref=dbSNP_129:rs21358830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046961.1	dbSNP	deletion	2401	2409	.	+	.	ID=3199;Variant_seq=-;Dbxref=dbSNP_129:rs53310215;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=CACATGTAT
AAAA02046961.1	dbSNP	SNV	2446	2446	.	+	.	ID=3200;Variant_seq=A;Dbxref=dbSNP_129:rs53499223;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046961.1	dbSNP	SNV	2469	2469	.	+	.	ID=3201;Variant_seq=A;Dbxref=dbSNP_129:rs53895040;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398369.1	dbSNP	SNV	176	176	.	+	.	ID=3202;Variant_seq=G;Dbxref=dbSNP_129:rs18663218;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398369.1	dbSNP	SNV	179	179	.	+	.	ID=3203;Variant_seq=A;Dbxref=dbSNP_129:rs18663227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398369.1	dbSNP	SNV	197	197	.	+	.	ID=3204;Variant_seq=G;Dbxref=dbSNP_129:rs18663236;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398369.1	dbSNP	SNV	248	248	.	+	.	ID=3205;Variant_seq=C;Dbxref=dbSNP_129:rs21325781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398369.1	dbSNP	SNV	1532	1532	.	+	.	ID=3206;Variant_seq=A;Dbxref=dbSNP_129:rs21285545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398369.1	dbSNP	SNV	3096	3096	.	+	.	ID=3207;Variant_seq=A;Dbxref=dbSNP_129:rs21285705;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398369.1	dbSNP	SNV	20470	20470	.	+	.	ID=3208;Variant_seq=A;Dbxref=dbSNP_129:rs20290879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044263.1	dbSNP	SNV	598	598	.	+	.	ID=3209;Variant_seq=T;Dbxref=dbSNP_129:rs53926153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044263.1	dbSNP	SNV	606	606	.	+	.	ID=3210;Variant_seq=A;Dbxref=dbSNP_129:rs52936072;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044263.1	dbSNP	SNV	611	611	.	+	.	ID=3211;Variant_seq=G;Dbxref=dbSNP_129:rs54080661;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044263.1	dbSNP	SNV	617	617	.	+	.	ID=3212;Variant_seq=C;Dbxref=dbSNP_129:rs53152587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044263.1	dbSNP	SNV	623	623	.	+	.	ID=3213;Variant_seq=A;Dbxref=dbSNP_129:rs52959046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044263.1	dbSNP	SNV	624	624	.	+	.	ID=3214;Variant_seq=T;Dbxref=dbSNP_129:rs52968504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044263.1	dbSNP	SNV	630	630	.	+	.	ID=3215;Variant_seq=G;Dbxref=dbSNP_129:rs53744091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044263.1	dbSNP	deletion	638	641	.	+	.	ID=3216;Variant_seq=-;Dbxref=dbSNP_129:rs53447517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=ACAA
AAAA02044263.1	dbSNP	SNV	643	643	.	+	.	ID=3217;Variant_seq=A;Dbxref=dbSNP_129:rs54172313;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040265.1	dbSNP	SNV	4309	4309	.	+	.	ID=3218;Variant_seq=C;Dbxref=dbSNP_129:rs19931110;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040265.1	dbSNP	SNV	4357	4357	.	+	.	ID=3219;Variant_seq=A;Dbxref=dbSNP_129:rs19931230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02040265.1	dbSNP	SNV	4400	4400	.	+	.	ID=3220;Variant_seq=T;Dbxref=dbSNP_129:rs53694290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048073.1	dbSNP	SNV	1359	1359	.	+	.	ID=3221;Variant_seq=C;Dbxref=dbSNP_129:rs52939656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02048073.1	dbSNP	SNV	1373	1373	.	+	.	ID=3222;Variant_seq=T;Dbxref=dbSNP_129:rs54231432;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048073.1	dbSNP	SNV	1424	1424	.	+	.	ID=3223;Variant_seq=A;Dbxref=dbSNP_129:rs54300162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02048073.1	dbSNP	SNV	1451	1451	.	+	.	ID=3224;Variant_seq=T;Dbxref=dbSNP_129:rs53031654;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048073.1	dbSNP	SNV	1457	1457	.	+	.	ID=3225;Variant_seq=T;Dbxref=dbSNP_129:rs53379779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02048073.1	dbSNP	SNV	1463	1463	.	+	.	ID=3226;Variant_seq=T;Dbxref=dbSNP_129:rs53711642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02042982.1	dbSNP	SNV	405	405	.	+	.	ID=3227;Variant_seq=A;Dbxref=dbSNP_129:rs54211593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02042982.1	dbSNP	SNV	1145	1145	.	+	.	ID=3228;Variant_seq=A;Dbxref=dbSNP_129:rs52969647;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	insertion	1851	1851	.	+	.	ID=3229;Variant_seq=T;Dbxref=dbSNP_129:rs53030774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1852	1852	.	+	.	ID=3230;Variant_seq=A;Dbxref=dbSNP_129:rs53844632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039958.1	dbSNP	insertion	1855	1855	.	+	.	ID=3231;Variant_seq=C;Dbxref=dbSNP_129:rs53646507;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1856	1856	.	+	.	ID=3232;Variant_seq=T;Dbxref=dbSNP_129:rs53319459;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	insertion	1856	1856	.	+	.	ID=3233;Variant_seq=T;Dbxref=dbSNP_129:rs53049000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1857	1857	.	+	.	ID=3234;Variant_seq=C;Dbxref=dbSNP_129:rs53268174;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039958.1	dbSNP	insertion	1857	1857	.	+	.	ID=3235;Variant_seq=T;Dbxref=dbSNP_129:rs53397649;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1858	1858	.	+	.	ID=3236;Variant_seq=T;Dbxref=dbSNP_129:rs52853443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1859	1859	.	+	.	ID=3237;Variant_seq=T;Dbxref=dbSNP_129:rs53283504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1860	1860	.	+	.	ID=3238;Variant_seq=A,T;Dbxref=dbSNP_129:rs54301288;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	SNV	1861	1861	.	+	.	ID=3239;Variant_seq=G;Dbxref=dbSNP_129:rs53624557;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1862	1862	.	+	.	ID=3240;Variant_seq=T;Dbxref=dbSNP_129:rs53555217;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	deletion	1862	1863	.	+	.	ID=3241;Variant_seq=-;Dbxref=dbSNP_129:rs53601497;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=GC
AAAA02039958.1	dbSNP	insertion	1863	1863	.	+	.	ID=3242;Variant_seq=C;Dbxref=dbSNP_129:rs53639223;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1864	1864	.	+	.	ID=3243;Variant_seq=G;Dbxref=dbSNP_129:rs54051842;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	insertion	1864	1864	.	+	.	ID=3244;Variant_seq=T;Dbxref=dbSNP_129:rs53293493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02039958.1	dbSNP	SNV	1866	1866	.	+	.	ID=3245;Variant_seq=T;Dbxref=dbSNP_129:rs53431089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1871	1871	.	+	.	ID=3246;Variant_seq=A;Dbxref=dbSNP_129:rs53000030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	SNV	1874	1874	.	+	.	ID=3247;Variant_seq=A;Dbxref=dbSNP_129:rs53568344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1876	1876	.	+	.	ID=3248;Variant_seq=A,C;Dbxref=dbSNP_129:rs53291310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	SNV	1879	1879	.	+	.	ID=3249;Variant_seq=T;Dbxref=dbSNP_129:rs54200577;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1880	1880	.	+	.	ID=3250;Variant_seq=C;Dbxref=dbSNP_129:rs53478739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039958.1	dbSNP	SNV	1884	1884	.	+	.	ID=3251;Variant_seq=A,C;Dbxref=dbSNP_129:rs53596865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	SNV	1886	1886	.	+	.	ID=3252;Variant_seq=T;Dbxref=dbSNP_129:rs53483800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039958.1	dbSNP	SNV	1888	1888	.	+	.	ID=3253;Variant_seq=T;Dbxref=dbSNP_129:rs53865220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1889	1889	.	+	.	ID=3254;Variant_seq=T;Dbxref=dbSNP_129:rs53893084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039958.1	dbSNP	SNV	1890	1890	.	+	.	ID=3255;Variant_seq=T,C;Dbxref=dbSNP_129:rs53035913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039958.1	dbSNP	SNV	1893	1893	.	+	.	ID=3256;Variant_seq=A,C,G;Dbxref=dbSNP_129:rs53035829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039958.1	dbSNP	SNV	1933	1933	.	+	.	ID=3257;Variant_seq=C,G;Dbxref=dbSNP_129:rs53567314;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039958.1	dbSNP	SNV	1940	1940	.	+	.	ID=3258;Variant_seq=T,C;Dbxref=dbSNP_129:rs54052301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398992.1	dbSNP	SNV	7372	7372	.	+	.	ID=3259;Variant_seq=A;Dbxref=dbSNP_129:rs19414902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398992.1	dbSNP	SNV	7373	7373	.	+	.	ID=3260;Variant_seq=G;Dbxref=dbSNP_129:rs19414892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050057.1	dbSNP	SNV	317	317	.	+	.	ID=3261;Variant_seq=C;Dbxref=dbSNP_129:rs18328739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02050057.1	dbSNP	SNV	1545	1545	.	+	.	ID=3262;Variant_seq=A;Dbxref=dbSNP_129:rs20321939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050057.1	dbSNP	SNV	1549	1549	.	+	.	ID=3263;Variant_seq=T;Dbxref=dbSNP_129:rs20321929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02050057.1	dbSNP	SNV	1684	1684	.	+	.	ID=3264;Variant_seq=T;Dbxref=dbSNP_129:rs20321889;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02050057.1	dbSNP	SNV	1719	1719	.	+	.	ID=3265;Variant_seq=T;Dbxref=dbSNP_129:rs20321879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050057.1	dbSNP	SNV	1720	1720	.	+	.	ID=3266;Variant_seq=C;Dbxref=dbSNP_129:rs20321869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050057.1	dbSNP	SNV	1857	1857	.	+	.	ID=3267;Variant_seq=G;Dbxref=dbSNP_129:rs20321829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050057.1	dbSNP	SNV	1883	1883	.	+	.	ID=3268;Variant_seq=T;Dbxref=dbSNP_129:rs20321809;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02050057.1	dbSNP	SNV	1886	1886	.	+	.	ID=3269;Variant_seq=C;Dbxref=dbSNP_129:rs20321799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02050057.1	dbSNP	SNV	1930	1930	.	+	.	ID=3270;Variant_seq=A;Dbxref=dbSNP_129:rs21503253;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045000.1	dbSNP	SNV	2078	2078	.	+	.	ID=3271;Variant_seq=T;Dbxref=dbSNP_129:rs53487984;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045000.1	dbSNP	SNV	2133	2133	.	+	.	ID=3272;Variant_seq=A;Dbxref=dbSNP_129:rs53135454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045000.1	dbSNP	SNV	2135	2135	.	+	.	ID=3273;Variant_seq=G;Dbxref=dbSNP_129:rs53772295;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045462.1	dbSNP	SNV	1636	1636	.	+	.	ID=3274;Variant_seq=C;Dbxref=dbSNP_129:rs53073103;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045462.1	dbSNP	SNV	1942	1942	.	+	.	ID=3275;Variant_seq=T;Dbxref=dbSNP_129:rs21507061;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046478.1	dbSNP	SNV	2016	2016	.	+	.	ID=3276;Variant_seq=A,C,G;Dbxref=dbSNP_129:rs17892066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02046478.1	dbSNP	SNV	2360	2360	.	+	.	ID=3277;Variant_seq=T;Dbxref=dbSNP_129:rs21071359;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046478.1	dbSNP	SNV	2544	2544	.	+	.	ID=3278;Variant_seq=T;Dbxref=dbSNP_129:rs21544415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02046478.1	dbSNP	SNV	2545	2545	.	+	.	ID=3279;Variant_seq=C;Dbxref=dbSNP_129:rs21544405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044169.1	dbSNP	SNV	2659	2659	.	+	.	ID=3280;Variant_seq=A;Dbxref=dbSNP_129:rs53602879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044169.1	dbSNP	SNV	2660	2660	.	+	.	ID=3281;Variant_seq=T;Dbxref=dbSNP_129:rs53143532;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	1848	1848	.	+	.	ID=3282;Variant_seq=G;Dbxref=dbSNP_129:rs21157648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399283.1	dbSNP	SNV	1851	1851	.	+	.	ID=3283;Variant_seq=A;Dbxref=dbSNP_129:rs21157638;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	1852	1852	.	+	.	ID=3284;Variant_seq=G;Dbxref=dbSNP_129:rs21157628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	2159	2159	.	+	.	ID=3285;Variant_seq=G;Dbxref=dbSNP_129:rs21157488;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399283.1	dbSNP	SNV	2187	2187	.	+	.	ID=3286;Variant_seq=A;Dbxref=dbSNP_129:rs21157478;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	2192	2192	.	+	.	ID=3287;Variant_seq=C;Dbxref=dbSNP_129:rs21157468;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399283.1	dbSNP	SNV	2193	2193	.	+	.	ID=3288;Variant_seq=T;Dbxref=dbSNP_129:rs21157458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	2212	2212	.	+	.	ID=3289;Variant_seq=T;Dbxref=dbSNP_129:rs21157448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	2218	2218	.	+	.	ID=3290;Variant_seq=G;Dbxref=dbSNP_129:rs21157417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399283.1	dbSNP	SNV	2220	2220	.	+	.	ID=3291;Variant_seq=A;Dbxref=dbSNP_129:rs21157407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	2223	2223	.	+	.	ID=3292;Variant_seq=T;Dbxref=dbSNP_129:rs21157397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	2254	2254	.	+	.	ID=3293;Variant_seq=G;Dbxref=dbSNP_129:rs21157377;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399283.1	dbSNP	SNV	2255	2255	.	+	.	ID=3294;Variant_seq=A;Dbxref=dbSNP_129:rs21157367;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	2286	2286	.	+	.	ID=3295;Variant_seq=T;Dbxref=dbSNP_129:rs21157357;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	2294	2294	.	+	.	ID=3296;Variant_seq=A;Dbxref=dbSNP_129:rs21157347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	4211	4211	.	+	.	ID=3297;Variant_seq=T;Dbxref=dbSNP_129:rs53057488;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399283.1	dbSNP	SNV	4216	4216	.	+	.	ID=3298;Variant_seq=T;Dbxref=dbSNP_129:rs53792213;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399283.1	dbSNP	SNV	4269	4269	.	+	.	ID=3299;Variant_seq=C;Dbxref=dbSNP_129:rs53824774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400326.1	dbSNP	SNV	70	70	.	+	.	ID=3300;Variant_seq=A;Dbxref=dbSNP_129:rs18068143;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400326.1	dbSNP	SNV	231	231	.	+	.	ID=3301;Variant_seq=T;Dbxref=dbSNP_129:rs18068161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400326.1	dbSNP	SNV	445	445	.	+	.	ID=3302;Variant_seq=T;Dbxref=dbSNP_129:rs52938245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH400326.1	dbSNP	SNV	446	446	.	+	.	ID=3303;Variant_seq=T;Dbxref=dbSNP_129:rs52897306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400326.1	dbSNP	SNV	453	453	.	+	.	ID=3304;Variant_seq=C;Dbxref=dbSNP_129:rs53388755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH400326.1	dbSNP	SNV	477	477	.	+	.	ID=3305;Variant_seq=G;Dbxref=dbSNP_129:rs53553682;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400326.1	dbSNP	SNV	504	504	.	+	.	ID=3306;Variant_seq=G;Dbxref=dbSNP_129:rs53885758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400326.1	dbSNP	SNV	2192	2192	.	+	.	ID=3307;Variant_seq=G;Dbxref=dbSNP_129:rs18687887;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH400326.1	dbSNP	SNV	2788	2788	.	+	.	ID=3308;Variant_seq=G;Dbxref=dbSNP_129:rs52983529;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400326.1	dbSNP	SNV	3160	3160	.	+	.	ID=3309;Variant_seq=G;Dbxref=dbSNP_129:rs54187797;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044092.1	dbSNP	SNV	152	152	.	+	.	ID=3310;Variant_seq=T;Dbxref=dbSNP_129:rs18030881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044092.1	dbSNP	SNV	178	178	.	+	.	ID=3311;Variant_seq=A;Dbxref=dbSNP_129:rs18030854;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044092.1	dbSNP	SNV	179	179	.	+	.	ID=3312;Variant_seq=T;Dbxref=dbSNP_129:rs18030845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044092.1	dbSNP	SNV	255	255	.	+	.	ID=3313;Variant_seq=T;Dbxref=dbSNP_129:rs18030836;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044092.1	dbSNP	SNV	1096	1096	.	+	.	ID=3314;Variant_seq=T;Dbxref=dbSNP_129:rs18030791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044092.1	dbSNP	SNV	1754	1754	.	+	.	ID=3315;Variant_seq=A;Dbxref=dbSNP_129:rs21195471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044092.1	dbSNP	SNV	2857	2857	.	+	.	ID=3316;Variant_seq=C;Dbxref=dbSNP_129:rs20195644;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044092.1	dbSNP	SNV	2858	2858	.	+	.	ID=3317;Variant_seq=T;Dbxref=dbSNP_129:rs20195634;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044092.1	dbSNP	SNV	2859	2859	.	+	.	ID=3318;Variant_seq=A;Dbxref=dbSNP_129:rs20195624;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044092.1	dbSNP	SNV	2865	2865	.	+	.	ID=3319;Variant_seq=A;Dbxref=dbSNP_129:rs20195594;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044092.1	dbSNP	SNV	2868	2868	.	+	.	ID=3320;Variant_seq=A;Dbxref=dbSNP_129:rs20195584;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044092.1	dbSNP	SNV	2873	2873	.	+	.	ID=3321;Variant_seq=C;Dbxref=dbSNP_129:rs20195554;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044092.1	dbSNP	SNV	2876	2876	.	+	.	ID=3322;Variant_seq=T;Dbxref=dbSNP_129:rs20195534;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044092.1	dbSNP	SNV	2877	2877	.	+	.	ID=3323;Variant_seq=C;Dbxref=dbSNP_129:rs20195524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401105.1	dbSNP	SNV	404	404	.	+	.	ID=3324;Variant_seq=C;Dbxref=dbSNP_129:rs20692703;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401105.1	dbSNP	SNV	405	405	.	+	.	ID=3325;Variant_seq=A;Dbxref=dbSNP_129:rs20692713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	578	578	.	+	.	ID=3326;Variant_seq=A;Dbxref=dbSNP_129:rs52883417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	767	767	.	+	.	ID=3327;Variant_seq=A;Dbxref=dbSNP_129:rs53593336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	1364	1364	.	+	.	ID=3328;Variant_seq=A;Dbxref=dbSNP_129:rs20695540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	1382	1382	.	+	.	ID=3329;Variant_seq=A;Dbxref=dbSNP_129:rs20695560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH401105.1	dbSNP	SNV	1388	1388	.	+	.	ID=3330;Variant_seq=A;Dbxref=dbSNP_129:rs20695570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	1403	1403	.	+	.	ID=3331;Variant_seq=A;Dbxref=dbSNP_129:rs20695580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	1404	1404	.	+	.	ID=3332;Variant_seq=T;Dbxref=dbSNP_129:rs20695590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401105.1	dbSNP	SNV	1412	1412	.	+	.	ID=3333;Variant_seq=G;Dbxref=dbSNP_129:rs20695600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401105.1	dbSNP	SNV	1430	1430	.	+	.	ID=3334;Variant_seq=A;Dbxref=dbSNP_129:rs20695610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH401105.1	dbSNP	SNV	1436	1436	.	+	.	ID=3335;Variant_seq=G;Dbxref=dbSNP_129:rs20695620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH401105.1	dbSNP	SNV	1443	1443	.	+	.	ID=3336;Variant_seq=T;Dbxref=dbSNP_129:rs20695630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH401105.1	dbSNP	SNV	1466	1466	.	+	.	ID=3337;Variant_seq=T;Dbxref=dbSNP_129:rs20695640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049834.1	dbSNP	SNV	1777	1777	.	+	.	ID=3338;Variant_seq=A;Dbxref=dbSNP_129:rs20692453;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02049834.1	dbSNP	SNV	1779	1779	.	+	.	ID=3339;Variant_seq=G;Dbxref=dbSNP_129:rs20692443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02049834.1	dbSNP	SNV	1788	1788	.	+	.	ID=3340;Variant_seq=C;Dbxref=dbSNP_129:rs20692433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040734.1	dbSNP	SNV	418	418	.	+	.	ID=3341;Variant_seq=G;Dbxref=dbSNP_129:rs19027378;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040734.1	dbSNP	SNV	431	431	.	+	.	ID=3342;Variant_seq=A;Dbxref=dbSNP_129:rs19027368;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040734.1	dbSNP	SNV	434	434	.	+	.	ID=3343;Variant_seq=A;Dbxref=dbSNP_129:rs19027358;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040734.1	dbSNP	SNV	468	468	.	+	.	ID=3344;Variant_seq=G;Dbxref=dbSNP_129:rs19027318;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040734.1	dbSNP	SNV	472	472	.	+	.	ID=3345;Variant_seq=A;Dbxref=dbSNP_129:rs19027308;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040734.1	dbSNP	SNV	496	496	.	+	.	ID=3346;Variant_seq=A;Dbxref=dbSNP_129:rs19027268;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02040734.1	dbSNP	SNV	498	498	.	+	.	ID=3347;Variant_seq=T;Dbxref=dbSNP_129:rs19027258;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040734.1	dbSNP	SNV	515	515	.	+	.	ID=3348;Variant_seq=G;Dbxref=dbSNP_129:rs19027228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02040734.1	dbSNP	SNV	540	540	.	+	.	ID=3349;Variant_seq=G;Dbxref=dbSNP_129:rs19027198;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037640.1	dbSNP	SNV	821	821	.	+	.	ID=3350;Variant_seq=T;Dbxref=dbSNP_129:rs18278121;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037640.1	dbSNP	SNV	866	866	.	+	.	ID=3351;Variant_seq=T;Dbxref=dbSNP_129:rs18278139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037640.1	dbSNP	SNV	1227	1227	.	+	.	ID=3352;Variant_seq=A;Dbxref=dbSNP_129:rs18278148;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037640.1	dbSNP	SNV	1319	1319	.	+	.	ID=3353;Variant_seq=T;Dbxref=dbSNP_129:rs18278157;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037640.1	dbSNP	SNV	1433	1433	.	+	.	ID=3354;Variant_seq=A;Dbxref=dbSNP_129:rs18278175;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037640.1	dbSNP	SNV	1775	1775	.	+	.	ID=3355;Variant_seq=A;Dbxref=dbSNP_129:rs18278193;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037640.1	dbSNP	SNV	2376	2376	.	+	.	ID=3356;Variant_seq=T;Dbxref=dbSNP_129:rs18749435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037640.1	dbSNP	SNV	3680	3680	.	+	.	ID=3357;Variant_seq=C;Dbxref=dbSNP_129:rs18270650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037640.1	dbSNP	SNV	6701	6701	.	+	.	ID=3358;Variant_seq=G;Dbxref=dbSNP_129:rs53509768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037640.1	dbSNP	SNV	6911	6911	.	+	.	ID=3359;Variant_seq=A;Dbxref=dbSNP_129:rs53969107;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045532.1	dbSNP	SNV	2483	2483	.	+	.	ID=3360;Variant_seq=A;Dbxref=dbSNP_129:rs18951798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3670	3670	.	+	.	ID=3361;Variant_seq=T;Dbxref=dbSNP_129:rs20933438;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399611.1	dbSNP	SNV	3702	3702	.	+	.	ID=3362;Variant_seq=T;Dbxref=dbSNP_129:rs53769730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3703	3703	.	+	.	ID=3363;Variant_seq=C;Dbxref=dbSNP_129:rs52989685;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399611.1	dbSNP	SNV	3704	3704	.	+	.	ID=3364;Variant_seq=T;Dbxref=dbSNP_129:rs53129460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3705	3705	.	+	.	ID=3365;Variant_seq=T;Dbxref=dbSNP_129:rs52928031;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3706	3706	.	+	.	ID=3366;Variant_seq=T;Dbxref=dbSNP_129:rs53945031;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3707	3707	.	+	.	ID=3367;Variant_seq=A;Dbxref=dbSNP_129:rs53847500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399611.1	dbSNP	SNV	3708	3708	.	+	.	ID=3368;Variant_seq=T;Dbxref=dbSNP_129:rs53327941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399611.1	dbSNP	SNV	3709	3709	.	+	.	ID=3369;Variant_seq=C;Dbxref=dbSNP_129:rs53170416;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399611.1	dbSNP	SNV	3711	3711	.	+	.	ID=3370;Variant_seq=C;Dbxref=dbSNP_129:rs53450475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399611.1	dbSNP	SNV	3714	3714	.	+	.	ID=3371;Variant_seq=T;Dbxref=dbSNP_129:rs52956744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3715	3715	.	+	.	ID=3372;Variant_seq=T,G;Dbxref=dbSNP_129:rs53478569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3716	3716	.	+	.	ID=3373;Variant_seq=T;Dbxref=dbSNP_129:rs54210304;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3717	3717	.	+	.	ID=3374;Variant_seq=A;Dbxref=dbSNP_129:rs53652683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399611.1	dbSNP	SNV	3719	3719	.	+	.	ID=3375;Variant_seq=C;Dbxref=dbSNP_129:rs53944839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399611.1	dbSNP	SNV	3720	3720	.	+	.	ID=3376;Variant_seq=T;Dbxref=dbSNP_129:rs54005016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3721	3721	.	+	.	ID=3377;Variant_seq=A;Dbxref=dbSNP_129:rs53419179;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3723	3723	.	+	.	ID=3378;Variant_seq=T;Dbxref=dbSNP_129:rs53916572;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3724	3724	.	+	.	ID=3379;Variant_seq=G;Dbxref=dbSNP_129:rs54364523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399611.1	dbSNP	SNV	3728	3728	.	+	.	ID=3380;Variant_seq=G;Dbxref=dbSNP_129:rs53830779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398681.1	dbSNP	SNV	1187	1187	.	+	.	ID=3381;Variant_seq=C;Dbxref=dbSNP_129:rs53880747;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398681.1	dbSNP	SNV	4981	4981	.	+	.	ID=3382;Variant_seq=C;Dbxref=dbSNP_129:rs18939503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398681.1	dbSNP	SNV	5056	5056	.	+	.	ID=3383;Variant_seq=C;Dbxref=dbSNP_129:rs19827589;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398681.1	dbSNP	SNV	5062	5062	.	+	.	ID=3384;Variant_seq=A;Dbxref=dbSNP_129:rs19827619;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398681.1	dbSNP	SNV	5063	5063	.	+	.	ID=3385;Variant_seq=A;Dbxref=dbSNP_129:rs19827629;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398681.1	dbSNP	SNV	5080	5080	.	+	.	ID=3386;Variant_seq=A;Dbxref=dbSNP_129:rs19827719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398681.1	dbSNP	SNV	5081	5081	.	+	.	ID=3387;Variant_seq=A;Dbxref=dbSNP_129:rs19827729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398681.1	dbSNP	SNV	5097	5097	.	+	.	ID=3388;Variant_seq=G;Dbxref=dbSNP_129:rs18939423;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398681.1	dbSNP	SNV	5106	5106	.	+	.	ID=3389;Variant_seq=T;Dbxref=dbSNP_129:rs18939413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH398681.1	dbSNP	SNV	5111	5111	.	+	.	ID=3390;Variant_seq=G;Dbxref=dbSNP_129:rs18939403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399235.1	dbSNP	SNV	172	172	.	+	.	ID=3391;Variant_seq=A;Dbxref=dbSNP_129:rs54222387;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038677.1	dbSNP	SNV	4312	4312	.	+	.	ID=3392;Variant_seq=G;Dbxref=dbSNP_129:rs20794074;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038677.1	dbSNP	SNV	5297	5297	.	+	.	ID=3393;Variant_seq=A;Dbxref=dbSNP_129:rs19527134;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038677.1	dbSNP	SNV	5581	5581	.	+	.	ID=3394;Variant_seq=A;Dbxref=dbSNP_129:rs20467544;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038677.1	dbSNP	SNV	6434	6434	.	+	.	ID=3395;Variant_seq=A;Dbxref=dbSNP_129:rs52960926;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038677.1	dbSNP	SNV	6486	6486	.	+	.	ID=3396;Variant_seq=A;Dbxref=dbSNP_129:rs54324872;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038677.1	dbSNP	SNV	6494	6494	.	+	.	ID=3397;Variant_seq=T;Dbxref=dbSNP_129:rs19432218;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038677.1	dbSNP	SNV	7215	7215	.	+	.	ID=3398;Variant_seq=A;Dbxref=dbSNP_129:rs20615185;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	116	116	.	+	.	ID=3399;Variant_seq=A;Dbxref=dbSNP_129:rs21325551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044479.1	dbSNP	SNV	119	119	.	+	.	ID=3400;Variant_seq=A;Dbxref=dbSNP_129:rs21325561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	124	124	.	+	.	ID=3401;Variant_seq=T;Dbxref=dbSNP_129:rs21325571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044479.1	dbSNP	SNV	131	131	.	+	.	ID=3402;Variant_seq=T;Dbxref=dbSNP_129:rs21325581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044479.1	dbSNP	SNV	132	132	.	+	.	ID=3403;Variant_seq=T;Dbxref=dbSNP_129:rs21325591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044479.1	dbSNP	SNV	142	142	.	+	.	ID=3404;Variant_seq=A;Dbxref=dbSNP_129:rs21325601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044479.1	dbSNP	SNV	173	173	.	+	.	ID=3405;Variant_seq=A;Dbxref=dbSNP_129:rs21325631;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044479.1	dbSNP	SNV	174	174	.	+	.	ID=3406;Variant_seq=G;Dbxref=dbSNP_129:rs21325641;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	180	180	.	+	.	ID=3407;Variant_seq=C;Dbxref=dbSNP_129:rs21325651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044479.1	dbSNP	SNV	200	200	.	+	.	ID=3408;Variant_seq=A;Dbxref=dbSNP_129:rs21325691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044479.1	dbSNP	SNV	209	209	.	+	.	ID=3409;Variant_seq=A;Dbxref=dbSNP_129:rs21325701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	1146	1146	.	+	.	ID=3410;Variant_seq=T;Dbxref=dbSNP_129:rs20645285;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	1270	1270	.	+	.	ID=3411;Variant_seq=G;Dbxref=dbSNP_129:rs21326991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044479.1	dbSNP	SNV	1271	1271	.	+	.	ID=3412;Variant_seq=G;Dbxref=dbSNP_129:rs21327001;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044479.1	dbSNP	SNV	1288	1288	.	+	.	ID=3413;Variant_seq=T;Dbxref=dbSNP_129:rs21327021;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044479.1	dbSNP	SNV	1330	1330	.	+	.	ID=3414;Variant_seq=G;Dbxref=dbSNP_129:rs21327161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044479.1	dbSNP	SNV	2702	2702	.	+	.	ID=3415;Variant_seq=A;Dbxref=dbSNP_129:rs21327521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399446.1	dbSNP	SNV	318	318	.	+	.	ID=3416;Variant_seq=T;Dbxref=dbSNP_129:rs53482546;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399446.1	dbSNP	SNV	323	323	.	+	.	ID=3417;Variant_seq=A;Dbxref=dbSNP_129:rs54358443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH399446.1	dbSNP	SNV	326	326	.	+	.	ID=3418;Variant_seq=C;Dbxref=dbSNP_129:rs53204611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399446.1	dbSNP	SNV	329	329	.	+	.	ID=3419;Variant_seq=T;Dbxref=dbSNP_129:rs52997340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02037039.1	dbSNP	SNV	4126	4126	.	+	.	ID=3420;Variant_seq=T;Dbxref=dbSNP_129:rs18703681;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02037039.1	dbSNP	SNV	4128	4128	.	+	.	ID=3421;Variant_seq=A,T,C;Dbxref=dbSNP_129:rs17899551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037039.1	dbSNP	SNV	4130	4130	.	+	.	ID=3422;Variant_seq=T;Dbxref=dbSNP_129:rs18703672;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044604.1	dbSNP	SNV	573	573	.	+	.	ID=3423;Variant_seq=G;Dbxref=dbSNP_129:rs20087445;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044604.1	dbSNP	SNV	588	588	.	+	.	ID=3424;Variant_seq=A;Dbxref=dbSNP_129:rs20087435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044604.1	dbSNP	SNV	710	710	.	+	.	ID=3425;Variant_seq=C;Dbxref=dbSNP_129:rs20087425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044604.1	dbSNP	SNV	730	730	.	+	.	ID=3426;Variant_seq=A;Dbxref=dbSNP_129:rs20087415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044604.1	dbSNP	SNV	827	827	.	+	.	ID=3427;Variant_seq=T;Dbxref=dbSNP_129:rs20087405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044604.1	dbSNP	SNV	858	858	.	+	.	ID=3428;Variant_seq=G;Dbxref=dbSNP_129:rs20087395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044604.1	dbSNP	SNV	1040	1040	.	+	.	ID=3429;Variant_seq=A;Dbxref=dbSNP_129:rs54137124;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044604.1	dbSNP	SNV	1079	1079	.	+	.	ID=3430;Variant_seq=G;Dbxref=dbSNP_129:rs54197713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044604.1	dbSNP	SNV	1081	1081	.	+	.	ID=3431;Variant_seq=A;Dbxref=dbSNP_129:rs53402464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044604.1	dbSNP	SNV	1085	1085	.	+	.	ID=3432;Variant_seq=T;Dbxref=dbSNP_129:rs53459930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044604.1	dbSNP	SNV	1309	1309	.	+	.	ID=3433;Variant_seq=G;Dbxref=dbSNP_129:rs20087385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044604.1	dbSNP	SNV	1312	1312	.	+	.	ID=3434;Variant_seq=G;Dbxref=dbSNP_129:rs20087375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044604.1	dbSNP	SNV	1317	1317	.	+	.	ID=3435;Variant_seq=T;Dbxref=dbSNP_129:rs20087365;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044604.1	dbSNP	SNV	1318	1318	.	+	.	ID=3436;Variant_seq=A;Dbxref=dbSNP_129:rs20087355;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044604.1	dbSNP	SNV	1333	1333	.	+	.	ID=3437;Variant_seq=A;Dbxref=dbSNP_129:rs20087345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	6880	6880	.	+	.	ID=3438;Variant_seq=C;Dbxref=dbSNP_129:rs19272468;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	15531	15531	.	+	.	ID=3439;Variant_seq=C;Dbxref=dbSNP_129:rs53483937;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	23805	23805	.	+	.	ID=3440;Variant_seq=A;Dbxref=dbSNP_129:rs21212434;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	23841	23841	.	+	.	ID=3441;Variant_seq=A;Dbxref=dbSNP_129:rs21212414;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	23846	23846	.	+	.	ID=3442;Variant_seq=A;Dbxref=dbSNP_129:rs21212404;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	23867	23867	.	+	.	ID=3443;Variant_seq=A;Dbxref=dbSNP_129:rs21212384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	23868	23868	.	+	.	ID=3444;Variant_seq=G;Dbxref=dbSNP_129:rs21212374;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	23869	23869	.	+	.	ID=3445;Variant_seq=A;Dbxref=dbSNP_129:rs21212364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	23941	23941	.	+	.	ID=3446;Variant_seq=T;Dbxref=dbSNP_129:rs21212344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	24519	24519	.	+	.	ID=3447;Variant_seq=C;Dbxref=dbSNP_129:rs21212274;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	24541	24541	.	+	.	ID=3448;Variant_seq=G;Dbxref=dbSNP_129:rs21212254;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	24545	24545	.	+	.	ID=3449;Variant_seq=G;Dbxref=dbSNP_129:rs21212244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	24555	24555	.	+	.	ID=3450;Variant_seq=T;Dbxref=dbSNP_129:rs21212234;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	24675	24675	.	+	.	ID=3451;Variant_seq=G;Dbxref=dbSNP_129:rs21212173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28081	28081	.	+	.	ID=3452;Variant_seq=A;Dbxref=dbSNP_129:rs21212073;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	28095	28095	.	+	.	ID=3453;Variant_seq=A;Dbxref=dbSNP_129:rs21212063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	28176	28176	.	+	.	ID=3454;Variant_seq=G;Dbxref=dbSNP_129:rs21212053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28251	28251	.	+	.	ID=3455;Variant_seq=T;Dbxref=dbSNP_129:rs21212033;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	28304	28304	.	+	.	ID=3456;Variant_seq=T;Dbxref=dbSNP_129:rs21212023;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28322	28322	.	+	.	ID=3457;Variant_seq=T;Dbxref=dbSNP_129:rs21212003;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28329	28329	.	+	.	ID=3458;Variant_seq=A;Dbxref=dbSNP_129:rs21211983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	28349	28349	.	+	.	ID=3459;Variant_seq=G;Dbxref=dbSNP_129:rs21211973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28371	28371	.	+	.	ID=3460;Variant_seq=A;Dbxref=dbSNP_129:rs21211953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	28394	28394	.	+	.	ID=3461;Variant_seq=C;Dbxref=dbSNP_129:rs21211943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	28395	28395	.	+	.	ID=3462;Variant_seq=C;Dbxref=dbSNP_129:rs21211933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	28396	28396	.	+	.	ID=3463;Variant_seq=C;Dbxref=dbSNP_129:rs21211923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	28398	28398	.	+	.	ID=3464;Variant_seq=T;Dbxref=dbSNP_129:rs21211913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28399	28399	.	+	.	ID=3465;Variant_seq=T;Dbxref=dbSNP_129:rs21211903;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28400	28400	.	+	.	ID=3466;Variant_seq=A;Dbxref=dbSNP_129:rs21211893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28401	28401	.	+	.	ID=3467;Variant_seq=A;Dbxref=dbSNP_129:rs21211883;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	28411	28411	.	+	.	ID=3468;Variant_seq=T;Dbxref=dbSNP_129:rs21211873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28419	28419	.	+	.	ID=3469;Variant_seq=T;Dbxref=dbSNP_129:rs21211863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28461	28461	.	+	.	ID=3470;Variant_seq=G;Dbxref=dbSNP_129:rs21211843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	28498	28498	.	+	.	ID=3471;Variant_seq=G;Dbxref=dbSNP_129:rs21211833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	28526	28526	.	+	.	ID=3472;Variant_seq=G;Dbxref=dbSNP_129:rs21211823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	29637	29637	.	+	.	ID=3473;Variant_seq=C;Dbxref=dbSNP_129:rs18322072;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035822.1	dbSNP	SNV	29639	29639	.	+	.	ID=3474;Variant_seq=T;Dbxref=dbSNP_129:rs18322081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	29646	29646	.	+	.	ID=3475;Variant_seq=T;Dbxref=dbSNP_129:rs18322090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02035822.1	dbSNP	SNV	29660	29660	.	+	.	ID=3476;Variant_seq=A;Dbxref=dbSNP_129:rs18322099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035822.1	dbSNP	SNV	29673	29673	.	+	.	ID=3477;Variant_seq=G;Dbxref=dbSNP_129:rs18322108;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02035822.1	dbSNP	SNV	29675	29675	.	+	.	ID=3478;Variant_seq=T;Dbxref=dbSNP_129:rs19471770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	279	279	.	+	.	ID=3479;Variant_seq=C;Dbxref=dbSNP_129:rs20086148;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043904.1	dbSNP	SNV	1385	1385	.	+	.	ID=3480;Variant_seq=A;Dbxref=dbSNP_129:rs20086531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043904.1	dbSNP	SNV	1388	1388	.	+	.	ID=3481;Variant_seq=C;Dbxref=dbSNP_129:rs20086541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043904.1	dbSNP	SNV	1389	1389	.	+	.	ID=3482;Variant_seq=A;Dbxref=dbSNP_129:rs20086551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043904.1	dbSNP	SNV	1391	1391	.	+	.	ID=3483;Variant_seq=T;Dbxref=dbSNP_129:rs20086561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1393	1393	.	+	.	ID=3484;Variant_seq=T;Dbxref=dbSNP_129:rs20086571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043904.1	dbSNP	SNV	1401	1401	.	+	.	ID=3485;Variant_seq=A;Dbxref=dbSNP_129:rs20086591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1402	1402	.	+	.	ID=3486;Variant_seq=G;Dbxref=dbSNP_129:rs20086601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043904.1	dbSNP	SNV	1403	1403	.	+	.	ID=3487;Variant_seq=C;Dbxref=dbSNP_129:rs20086611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043904.1	dbSNP	SNV	1404	1404	.	+	.	ID=3488;Variant_seq=T;Dbxref=dbSNP_129:rs20086621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043904.1	dbSNP	SNV	1495	1495	.	+	.	ID=3489;Variant_seq=G;Dbxref=dbSNP_129:rs20086811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1496	1496	.	+	.	ID=3490;Variant_seq=T;Dbxref=dbSNP_129:rs20086821;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02043904.1	dbSNP	SNV	1501	1501	.	+	.	ID=3491;Variant_seq=T;Dbxref=dbSNP_129:rs20086831;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1504	1504	.	+	.	ID=3492;Variant_seq=G;Dbxref=dbSNP_129:rs20086841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1525	1525	.	+	.	ID=3493;Variant_seq=T;Dbxref=dbSNP_129:rs20086870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043904.1	dbSNP	SNV	1576	1576	.	+	.	ID=3494;Variant_seq=T;Dbxref=dbSNP_129:rs20086890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02047934.1	dbSNP	SNV	1631	1631	.	+	.	ID=3495;Variant_seq=A;Dbxref=dbSNP_129:rs18121811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02047934.1	dbSNP	SNV	2075	2075	.	+	.	ID=3496;Variant_seq=T;Dbxref=dbSNP_129:rs20957414;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02047934.1	dbSNP	SNV	2091	2091	.	+	.	ID=3497;Variant_seq=C;Dbxref=dbSNP_129:rs20957384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399884.1	dbSNP	SNV	1223	1223	.	+	.	ID=3498;Variant_seq=G;Dbxref=dbSNP_129:rs53958186;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039965.1	dbSNP	SNV	543	543	.	+	.	ID=3499;Variant_seq=A,C,G;Dbxref=dbSNP_129:rs17892066;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039965.1	dbSNP	SNV	1382	1382	.	+	.	ID=3500;Variant_seq=T;Dbxref=dbSNP_129:rs52986087;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039965.1	dbSNP	SNV	1446	1446	.	+	.	ID=3501;Variant_seq=T;Dbxref=dbSNP_129:rs52901691;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039965.1	dbSNP	SNV	1466	1466	.	+	.	ID=3502;Variant_seq=G;Dbxref=dbSNP_129:rs54005118;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039965.1	dbSNP	SNV	1490	1490	.	+	.	ID=3503;Variant_seq=T;Dbxref=dbSNP_129:rs52990987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02039965.1	dbSNP	SNV	1788	1788	.	+	.	ID=3504;Variant_seq=G;Dbxref=dbSNP_129:rs19373822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039965.1	dbSNP	SNV	2228	2228	.	+	.	ID=3505;Variant_seq=G;Dbxref=dbSNP_129:rs54392989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039965.1	dbSNP	SNV	4503	4503	.	+	.	ID=3506;Variant_seq=G;Dbxref=dbSNP_129:rs20994580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037514.1	dbSNP	SNV	419	419	.	+	.	ID=3507;Variant_seq=A;Dbxref=dbSNP_129:rs19897199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037514.1	dbSNP	SNV	425	425	.	+	.	ID=3508;Variant_seq=A,T,C;Dbxref=dbSNP_129:rs17903606;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02037514.1	dbSNP	SNV	756	756	.	+	.	ID=3509;Variant_seq=C;Dbxref=dbSNP_129:rs19625130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02037514.1	dbSNP	SNV	10036	10036	.	+	.	ID=3510;Variant_seq=T;Dbxref=dbSNP_129:rs53368322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038130.1	dbSNP	SNV	4034	4034	.	+	.	ID=3511;Variant_seq=A;Dbxref=dbSNP_129:rs21003767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038130.1	dbSNP	SNV	4109	4109	.	+	.	ID=3512;Variant_seq=A;Dbxref=dbSNP_129:rs21003707;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038130.1	dbSNP	SNV	4161	4161	.	+	.	ID=3513;Variant_seq=A;Dbxref=dbSNP_129:rs21003617;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4165	4165	.	+	.	ID=3514;Variant_seq=C;Dbxref=dbSNP_129:rs21003607;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4166	4166	.	+	.	ID=3515;Variant_seq=A;Dbxref=dbSNP_129:rs21003597;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038130.1	dbSNP	SNV	4167	4167	.	+	.	ID=3516;Variant_seq=C;Dbxref=dbSNP_129:rs21003587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4168	4168	.	+	.	ID=3517;Variant_seq=C;Dbxref=dbSNP_129:rs21003577;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038130.1	dbSNP	SNV	4169	4169	.	+	.	ID=3518;Variant_seq=C;Dbxref=dbSNP_129:rs21003567;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4238	4238	.	+	.	ID=3519;Variant_seq=T;Dbxref=dbSNP_129:rs21003537;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038130.1	dbSNP	SNV	4240	4240	.	+	.	ID=3520;Variant_seq=C;Dbxref=dbSNP_129:rs21003527;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4243	4243	.	+	.	ID=3521;Variant_seq=A;Dbxref=dbSNP_129:rs21003517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038130.1	dbSNP	SNV	4273	4273	.	+	.	ID=3522;Variant_seq=C;Dbxref=dbSNP_129:rs21003497;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4282	4282	.	+	.	ID=3523;Variant_seq=G;Dbxref=dbSNP_129:rs21003487;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02038130.1	dbSNP	SNV	4285	4285	.	+	.	ID=3524;Variant_seq=G;Dbxref=dbSNP_129:rs21003477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038130.1	dbSNP	SNV	4292	4292	.	+	.	ID=3525;Variant_seq=C;Dbxref=dbSNP_129:rs21003467;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02038071.1	dbSNP	SNV	6669	6669	.	+	.	ID=3526;Variant_seq=T;Dbxref=dbSNP_129:rs19060621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038071.1	dbSNP	SNV	7671	7671	.	+	.	ID=3527;Variant_seq=A;Dbxref=dbSNP_129:rs20481077;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02038071.1	dbSNP	SNV	8558	8558	.	+	.	ID=3528;Variant_seq=T;Dbxref=dbSNP_129:rs53026865;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398949.1	dbSNP	SNV	1636	1636	.	+	.	ID=3529;Variant_seq=G;Dbxref=dbSNP_129:rs19265681;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398949.1	dbSNP	SNV	2544	2544	.	+	.	ID=3530;Variant_seq=T;Dbxref=dbSNP_129:rs19350779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398949.1	dbSNP	SNV	5950	5950	.	+	.	ID=3531;Variant_seq=A;Dbxref=dbSNP_129:rs53114710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
CH398949.1	dbSNP	SNV	5951	5951	.	+	.	ID=3532;Variant_seq=A;Dbxref=dbSNP_129:rs53800203;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	199	199	.	+	.	ID=3533;Variant_seq=T;Dbxref=dbSNP_129:rs54004493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045744.1	dbSNP	SNV	248	248	.	+	.	ID=3534;Variant_seq=C;Dbxref=dbSNP_129:rs54395843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	249	249	.	+	.	ID=3535;Variant_seq=T;Dbxref=dbSNP_129:rs53155332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045744.1	dbSNP	SNV	266	266	.	+	.	ID=3536;Variant_seq=A;Dbxref=dbSNP_129:rs53753396;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045744.1	dbSNP	deletion	273	273	.	+	.	ID=3537;Variant_seq=-;Dbxref=dbSNP_129:rs54044608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	insertion	280	280	.	+	.	ID=3538;Variant_seq=T;Dbxref=dbSNP_129:rs54398000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02045744.1	dbSNP	insertion	281	281	.	+	.	ID=3539;Variant_seq=T;Dbxref=dbSNP_129:rs53152477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
AAAA02045744.1	dbSNP	SNV	282	282	.	+	.	ID=3540;Variant_seq=T;Dbxref=dbSNP_129:rs54214075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	deletion	286	286	.	+	.	ID=3541;Variant_seq=-;Dbxref=dbSNP_129:rs53531666;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	288	288	.	+	.	ID=3542;Variant_seq=T;Dbxref=dbSNP_129:rs53741639;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02045744.1	dbSNP	SNV	293	293	.	+	.	ID=3543;Variant_seq=C;Dbxref=dbSNP_129:rs54367475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	302	302	.	+	.	ID=3544;Variant_seq=T;Dbxref=dbSNP_129:rs54141803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	306	306	.	+	.	ID=3545;Variant_seq=A;Dbxref=dbSNP_129:rs52996861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045744.1	dbSNP	SNV	307	307	.	+	.	ID=3546;Variant_seq=C;Dbxref=dbSNP_129:rs53885822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02045744.1	dbSNP	SNV	310	310	.	+	.	ID=3547;Variant_seq=A;Dbxref=dbSNP_129:rs54094990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	315	315	.	+	.	ID=3548;Variant_seq=T;Dbxref=dbSNP_129:rs54288403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	323	323	.	+	.	ID=3549;Variant_seq=A;Dbxref=dbSNP_129:rs54083079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	324	324	.	+	.	ID=3550;Variant_seq=A;Dbxref=dbSNP_129:rs53737010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	406	406	.	+	.	ID=3551;Variant_seq=T;Dbxref=dbSNP_129:rs53692895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	408	408	.	+	.	ID=3552;Variant_seq=T;Dbxref=dbSNP_129:rs54051913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02045744.1	dbSNP	SNV	413	413	.	+	.	ID=3553;Variant_seq=C;Dbxref=dbSNP_129:rs53584727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02045744.1	dbSNP	SNV	426	426	.	+	.	ID=3554;Variant_seq=A;Dbxref=dbSNP_129:rs53854574;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043699.1	dbSNP	SNV	1669	1669	.	+	.	ID=3555;Variant_seq=G;Dbxref=dbSNP_129:rs20283168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02043699.1	dbSNP	SNV	2431	2431	.	+	.	ID=3556;Variant_seq=A;Dbxref=dbSNP_129:rs53139112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02038700.1	dbSNP	SNV	3844	3844	.	+	.	ID=3557;Variant_seq=C;Dbxref=dbSNP_129:rs21424495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039298.1	dbSNP	SNV	50	50	.	+	.	ID=3558;Variant_seq=C;Dbxref=dbSNP_129:rs19999376;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039298.1	dbSNP	SNV	2796	2796	.	+	.	ID=3559;Variant_seq=A;Dbxref=dbSNP_129:rs53432559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039298.1	dbSNP	SNV	3793	3793	.	+	.	ID=3560;Variant_seq=G;Dbxref=dbSNP_129:rs21393855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039298.1	dbSNP	SNV	3796	3796	.	+	.	ID=3561;Variant_seq=A;Dbxref=dbSNP_129:rs21393845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02039298.1	dbSNP	SNV	3814	3814	.	+	.	ID=3562;Variant_seq=G;Dbxref=dbSNP_129:rs21393835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02039298.1	dbSNP	SNV	3820	3820	.	+	.	ID=3563;Variant_seq=C;Dbxref=dbSNP_129:rs21393825;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039298.1	dbSNP	SNV	3823	3823	.	+	.	ID=3564;Variant_seq=C;Dbxref=dbSNP_129:rs21393815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02039298.1	dbSNP	SNV	3824	3824	.	+	.	ID=3565;Variant_seq=A;Dbxref=dbSNP_129:rs21393805;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043950.1	dbSNP	SNV	1608	1608	.	+	.	ID=3566;Variant_seq=T;Dbxref=dbSNP_129:rs54224042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043950.1	dbSNP	SNV	1745	1745	.	+	.	ID=3567;Variant_seq=A;Dbxref=dbSNP_129:rs54374410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043950.1	dbSNP	SNV	1766	1766	.	+	.	ID=3568;Variant_seq=A;Dbxref=dbSNP_129:rs52875559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02043950.1	dbSNP	SNV	1907	1907	.	+	.	ID=3569;Variant_seq=A;Dbxref=dbSNP_129:rs52858134;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043950.1	dbSNP	SNV	1917	1917	.	+	.	ID=3570;Variant_seq=A;Dbxref=dbSNP_129:rs53900763;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02043950.1	dbSNP	SNV	2264	2264	.	+	.	ID=3571;Variant_seq=T;Dbxref=dbSNP_129:rs53184653;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044212.1	dbSNP	SNV	1837	1837	.	+	.	ID=3572;Variant_seq=C;Dbxref=dbSNP_129:rs53325786;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044212.1	dbSNP	SNV	1838	1838	.	+	.	ID=3573;Variant_seq=A;Dbxref=dbSNP_129:rs53537734;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044212.1	dbSNP	SNV	1841	1841	.	+	.	ID=3574;Variant_seq=T;Dbxref=dbSNP_129:rs53350475;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044212.1	dbSNP	SNV	1843	1843	.	+	.	ID=3575;Variant_seq=T;Dbxref=dbSNP_129:rs54175136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044212.1	dbSNP	SNV	1844	1844	.	+	.	ID=3576;Variant_seq=C;Dbxref=dbSNP_129:rs53616793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02044212.1	dbSNP	SNV	1917	1917	.	+	.	ID=3577;Variant_seq=C;Dbxref=dbSNP_129:rs53555042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044905.1	dbSNP	SNV	1868	1868	.	+	.	ID=3578;Variant_seq=T;Dbxref=dbSNP_129:rs21761452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
AAAA02044905.1	dbSNP	SNV	2345	2345	.	+	.	ID=3579;Variant_seq=G;Dbxref=dbSNP_129:rs54139674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02044905.1	dbSNP	SNV	2348	2348	.	+	.	ID=3580;Variant_seq=A;Dbxref=dbSNP_129:rs53767385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02044905.1	dbSNP	SNV	2364	2364	.	+	.	ID=3581;Variant_seq=A;Dbxref=dbSNP_129:rs53746988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02046603.1	dbSNP	SNV	1126	1126	.	+	.	ID=3582;Variant_seq=T;Dbxref=dbSNP_129:rs53892653;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
CH399816.1	dbSNP	SNV	4271	4271	.	+	.	ID=3583;Variant_seq=C;Dbxref=dbSNP_129:rs21185100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH399763.1	dbSNP	SNV	1969	1969	.	+	.	ID=3584;Variant_seq=C;Dbxref=dbSNP_129:rs20771605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
AAAA02035869.1	dbSNP	SNV	10955	10955	.	+	.	ID=3585;Variant_seq=C;Dbxref=dbSNP_129:rs20065179;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
AAAA02035869.1	dbSNP	SNV	18874	18874	.	+	.	ID=3586;Variant_seq=G;Dbxref=dbSNP_129:rs20336368;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH400737.1	dbSNP	SNV	901	901	.	+	.	ID=3587;Variant_seq=G;Dbxref=dbSNP_129:rs21156783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040742.1	dbSNP	SNV	77	77	.	+	.	ID=3588;Variant_seq=G;Dbxref=dbSNP_129:rs18335731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
AAAA02040742.1	dbSNP	SNV	241	241	.	+	.	ID=3589;Variant_seq=C;Dbxref=dbSNP_129:rs19103790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399418.1	dbSNP	SNV	1808	1808	.	+	.	ID=3590;Variant_seq=G;Dbxref=dbSNP_129:rs19019850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH399418.1	dbSNP	SNV	2060	2060	.	+	.	ID=3591;Variant_seq=C;Dbxref=dbSNP_129:rs20935677;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
CH398680.1	dbSNP	SNV	10718	10718	.	+	.	ID=3592;Variant_seq=G;Dbxref=dbSNP_129:rs19693657;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
CH398680.1	dbSNP	SNV	10719	10719	.	+	.	ID=3593;Variant_seq=T;Dbxref=dbSNP_129:rs19693647;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	992	992	.	+	.	ID=3594;Variant_seq=G;Dbxref=dbSNP_129:rs18939204;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1129	1129	.	+	.	ID=3595;Variant_seq=G;Dbxref=dbSNP_129:rs18939214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1184	1184	.	+	.	ID=3596;Variant_seq=C;Dbxref=dbSNP_129:rs18939224;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1320	1320	.	+	.	ID=3597;Variant_seq=T;Dbxref=dbSNP_129:rs18939234;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1622	1622	.	+	.	ID=3598;Variant_seq=T;Dbxref=dbSNP_129:rs18939244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1669	1669	.	+	.	ID=3599;Variant_seq=T;Dbxref=dbSNP_129:rs18939254;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1760	1760	.	+	.	ID=3600;Variant_seq=A;Dbxref=dbSNP_129:rs18939264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1814	1814	.	+	.	ID=3601;Variant_seq=T;Dbxref=dbSNP_129:rs18939274;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	8361	8361	.	+	.	ID=3602;Variant_seq=T;Dbxref=dbSNP_129:rs54411912;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	9517	9517	.	+	.	ID=3603;Variant_seq=A;Dbxref=dbSNP_129:rs17918397;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	10282	10282	.	+	.	ID=3604;Variant_seq=G;Dbxref=dbSNP_129:rs18045443;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	11387	11387	.	+	.	ID=3605;Variant_seq=A;Dbxref=dbSNP_129:rs17917965;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	11400	11400	.	+	.	ID=3606;Variant_seq=A;Dbxref=dbSNP_129:rs17917956;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	12371	12371	.	+	.	ID=3607;Variant_seq=G;Dbxref=dbSNP_129:rs19671580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	19738	19738	.	+	.	ID=3608;Variant_seq=T;Dbxref=dbSNP_129:rs18938884;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	19740	19740	.	+	.	ID=3609;Variant_seq=G;Dbxref=dbSNP_129:rs18938894;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	19741	19741	.	+	.	ID=3610;Variant_seq=G;Dbxref=dbSNP_129:rs18938904;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	19744	19744	.	+	.	ID=3611;Variant_seq=A;Dbxref=dbSNP_129:rs18938914;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	20309	20309	.	+	.	ID=3612;Variant_seq=A;Dbxref=dbSNP_129:rs18938914;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	20312	20312	.	+	.	ID=3613;Variant_seq=G;Dbxref=dbSNP_129:rs18938904;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	20313	20313	.	+	.	ID=3614;Variant_seq=G;Dbxref=dbSNP_129:rs18938894;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	20315	20315	.	+	.	ID=3615;Variant_seq=T;Dbxref=dbSNP_129:rs18938884;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	24142	24142	.	+	.	ID=3616;Variant_seq=A;Dbxref=dbSNP_129:rs18939204;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	24280	24280	.	+	.	ID=3617;Variant_seq=A;Dbxref=dbSNP_129:rs18939214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	24335	24335	.	+	.	ID=3618;Variant_seq=A;Dbxref=dbSNP_129:rs18939224;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	24471	24471	.	+	.	ID=3619;Variant_seq=C;Dbxref=dbSNP_129:rs18939234;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	24773	24773	.	+	.	ID=3620;Variant_seq=C;Dbxref=dbSNP_129:rs18939244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	24820	24820	.	+	.	ID=3621;Variant_seq=C;Dbxref=dbSNP_129:rs18939254;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	24911	24911	.	+	.	ID=3622;Variant_seq=G;Dbxref=dbSNP_129:rs18939264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	24965	24965	.	+	.	ID=3623;Variant_seq=C;Dbxref=dbSNP_129:rs18939274;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	29890	29890	.	+	.	ID=3624;Variant_seq=C;Dbxref=dbSNP_129:rs18939514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	29949	29949	.	+	.	ID=3625;Variant_seq=G;Dbxref=dbSNP_129:rs18939524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	30259	30259	.	+	.	ID=3626;Variant_seq=A;Dbxref=dbSNP_129:rs18939614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	35208	35208	.	+	.	ID=3627;Variant_seq=T;Dbxref=dbSNP_129:rs18939514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	35267	35267	.	+	.	ID=3628;Variant_seq=A;Dbxref=dbSNP_129:rs18939524;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	35578	35578	.	+	.	ID=3629;Variant_seq=C;Dbxref=dbSNP_129:rs18939614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	40249	40249	.	+	.	ID=3630;Variant_seq=A;Dbxref=dbSNP_129:rs20427280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	40250	40250	.	+	.	ID=3631;Variant_seq=T;Dbxref=dbSNP_129:rs20427290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	40251	40251	.	+	.	ID=3632;Variant_seq=A;Dbxref=dbSNP_129:rs20427300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	40252	40252	.	+	.	ID=3633;Variant_seq=G;Dbxref=dbSNP_129:rs20427310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	40271	40271	.	+	.	ID=3634;Variant_seq=G;Dbxref=dbSNP_129:rs18940113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	40837	40837	.	+	.	ID=3635;Variant_seq=A;Dbxref=dbSNP_129:rs20430286;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	41035	41035	.	+	.	ID=3636;Variant_seq=T;Dbxref=dbSNP_129:rs19123448;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	41910	41910	.	+	.	ID=3637;Variant_seq=A;Dbxref=dbSNP_129:rs18940723;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	42911	42911	.	+	.	ID=3638;Variant_seq=C;Dbxref=dbSNP_129:rs18940972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	53528	53528	.	+	.	ID=3639;Variant_seq=C;Dbxref=dbSNP_129:rs18941742;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	61534	61534	.	+	.	ID=3640;Variant_seq=T;Dbxref=dbSNP_129:rs20452835;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	61540	61540	.	+	.	ID=3641;Variant_seq=G;Dbxref=dbSNP_129:rs20452825;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	61541	61541	.	+	.	ID=3642;Variant_seq=G;Dbxref=dbSNP_129:rs20452815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	70707	70707	.	+	.	ID=3643;Variant_seq=G;Dbxref=dbSNP_129:rs20422171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	70708	70708	.	+	.	ID=3644;Variant_seq=T;Dbxref=dbSNP_129:rs20422181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	71290	71290	.	+	.	ID=3645;Variant_seq=C;Dbxref=dbSNP_129:rs18942497;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	92428	92428	.	+	.	ID=3646;Variant_seq=G;Dbxref=dbSNP_129:rs18941742;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	103488	103488	.	+	.	ID=3647;Variant_seq=G;Dbxref=dbSNP_129:rs18943998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	103608	103608	.	+	.	ID=3648;Variant_seq=A;Dbxref=dbSNP_129:rs18944008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	103812	103812	.	+	.	ID=3649;Variant_seq=T;Dbxref=dbSNP_129:rs18944028;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	103918	103918	.	+	.	ID=3650;Variant_seq=T;Dbxref=dbSNP_129:rs18944048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	104120	104120	.	+	.	ID=3651;Variant_seq=C;Dbxref=dbSNP_129:rs18944078;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	104399	104399	.	+	.	ID=3652;Variant_seq=T;Dbxref=dbSNP_129:rs18944098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	105334	105334	.	+	.	ID=3653;Variant_seq=C;Dbxref=dbSNP_129:rs18943718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	105849	105849	.	+	.	ID=3654;Variant_seq=C;Dbxref=dbSNP_129:rs18093964;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	108098	108098	.	+	.	ID=3655;Variant_seq=G;Dbxref=dbSNP_129:rs18943998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	108218	108218	.	+	.	ID=3656;Variant_seq=A;Dbxref=dbSNP_129:rs18944008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	108422	108422	.	+	.	ID=3657;Variant_seq=T;Dbxref=dbSNP_129:rs18944028;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	108528	108528	.	+	.	ID=3658;Variant_seq=T;Dbxref=dbSNP_129:rs18944048;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	108730	108730	.	+	.	ID=3659;Variant_seq=T;Dbxref=dbSNP_129:rs18944078;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	109008	109008	.	+	.	ID=3660;Variant_seq=G;Dbxref=dbSNP_129:rs18944098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	109934	109934	.	+	.	ID=3661;Variant_seq=G;Dbxref=dbSNP_129:rs18943718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	110142	110142	.	+	.	ID=3662;Variant_seq=T;Dbxref=dbSNP_129:rs18944168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	110159	110159	.	+	.	ID=3663;Variant_seq=T;Dbxref=dbSNP_129:rs18944178;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	110163	110163	.	+	.	ID=3664;Variant_seq=T;Dbxref=dbSNP_129:rs18944188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	110167	110167	.	+	.	ID=3665;Variant_seq=A;Dbxref=dbSNP_129:rs18944198;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	110179	110179	.	+	.	ID=3666;Variant_seq=C;Dbxref=dbSNP_129:rs18944208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	110199	110199	.	+	.	ID=3667;Variant_seq=T;Dbxref=dbSNP_129:rs18944228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	110383	110383	.	+	.	ID=3668;Variant_seq=T;Dbxref=dbSNP_129:rs18944168;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	110400	110400	.	+	.	ID=3669;Variant_seq=T;Dbxref=dbSNP_129:rs18944178;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	110404	110404	.	+	.	ID=3670;Variant_seq=T;Dbxref=dbSNP_129:rs18944188;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	110408	110408	.	+	.	ID=3671;Variant_seq=A;Dbxref=dbSNP_129:rs18944198;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	110420	110420	.	+	.	ID=3672;Variant_seq=C;Dbxref=dbSNP_129:rs18944208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	110440	110440	.	+	.	ID=3673;Variant_seq=T;Dbxref=dbSNP_129:rs18944228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	111660	111660	.	+	.	ID=3674;Variant_seq=T;Dbxref=dbSNP_129:rs18944938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	111661	111661	.	+	.	ID=3675;Variant_seq=T;Dbxref=dbSNP_129:rs18944948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	119975	119975	.	+	.	ID=3676;Variant_seq=T;Dbxref=dbSNP_129:rs54142596;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	119978	119978	.	+	.	ID=3677;Variant_seq=T;Dbxref=dbSNP_129:rs52953832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	119987	119987	.	+	.	ID=3678;Variant_seq=A;Dbxref=dbSNP_129:rs52849589;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	173038	173038	.	+	.	ID=3679;Variant_seq=G;Dbxref=dbSNP_129:rs18947849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	177728	177728	.	+	.	ID=3680;Variant_seq=C;Dbxref=dbSNP_129:rs53114987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	177961	177961	.	+	.	ID=3681;Variant_seq=G;Dbxref=dbSNP_129:rs54192483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	177963	177963	.	+	.	ID=3682;Variant_seq=G;Dbxref=dbSNP_129:rs54120454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	178220	178220	.	+	.	ID=3683;Variant_seq=G;Dbxref=dbSNP_129:rs53149523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	178583	178583	.	+	.	ID=3684;Variant_seq=A;Dbxref=dbSNP_129:rs53240284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	179479	179479	.	+	.	ID=3685;Variant_seq=C;Dbxref=dbSNP_129:rs52898339;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	188991	188991	.	+	.	ID=3686;Variant_seq=G;Dbxref=dbSNP_129:rs18947849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	189494	189494	.	+	.	ID=3687;Variant_seq=C;Dbxref=dbSNP_129:rs52898339;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	190986	190986	.	+	.	ID=3688;Variant_seq=C;Dbxref=dbSNP_129:rs53114987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	191218	191218	.	+	.	ID=3689;Variant_seq=G;Dbxref=dbSNP_129:rs54192483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	191220	191220	.	+	.	ID=3690;Variant_seq=G;Dbxref=dbSNP_129:rs54120454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	191483	191483	.	+	.	ID=3691;Variant_seq=G;Dbxref=dbSNP_129:rs53149523;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	191846	191846	.	+	.	ID=3692;Variant_seq=C;Dbxref=dbSNP_129:rs53240284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	194535	194535	.	+	.	ID=3693;Variant_seq=A;Dbxref=dbSNP_129:rs18012939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	222762	222762	.	+	.	ID=3694;Variant_seq=A;Dbxref=dbSNP_129:rs52933026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	222765	222765	.	+	.	ID=3695;Variant_seq=G;Dbxref=dbSNP_129:rs54314987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	222768	222768	.	+	.	ID=3696;Variant_seq=C;Dbxref=dbSNP_129:rs54086613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	222783	222783	.	+	.	ID=3697;Variant_seq=T;Dbxref=dbSNP_129:rs54013767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	225351	225351	.	+	.	ID=3698;Variant_seq=C;Dbxref=dbSNP_129:rs21572966;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	226774	226774	.	+	.	ID=3699;Variant_seq=C;Dbxref=dbSNP_129:rs21106312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	226800	226800	.	+	.	ID=3700;Variant_seq=C;Dbxref=dbSNP_129:rs21106342;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	227520	227520	.	+	.	ID=3701;Variant_seq=C;Dbxref=dbSNP_129:rs21572966;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	244081	244081	.	+	.	ID=3702;Variant_seq=G;Dbxref=dbSNP_129:rs18951262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	244354	244354	.	+	.	ID=3703;Variant_seq=C;Dbxref=dbSNP_129:rs18951332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	244544	244544	.	+	.	ID=3704;Variant_seq=T;Dbxref=dbSNP_129:rs18951372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	247312	247312	.	+	.	ID=3705;Variant_seq=G;Dbxref=dbSNP_129:rs18951422;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	247473	247473	.	+	.	ID=3706;Variant_seq=A;Dbxref=dbSNP_129:rs18951442;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	247713	247713	.	+	.	ID=3707;Variant_seq=A;Dbxref=dbSNP_129:rs18951472;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	247951	247951	.	+	.	ID=3708;Variant_seq=T;Dbxref=dbSNP_129:rs18951542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	259899	259899	.	+	.	ID=3709;Variant_seq=C;Dbxref=dbSNP_129:rs18952102;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	263085	263085	.	+	.	ID=3710;Variant_seq=T;Dbxref=dbSNP_129:rs18952382;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	264041	264041	.	+	.	ID=3711;Variant_seq=C;Dbxref=dbSNP_129:rs18951262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	264314	264314	.	+	.	ID=3712;Variant_seq=G;Dbxref=dbSNP_129:rs18951332;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	264504	264504	.	+	.	ID=3713;Variant_seq=C;Dbxref=dbSNP_129:rs18951372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	264981	264981	.	+	.	ID=3714;Variant_seq=C;Dbxref=dbSNP_129:rs18951422;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	265142	265142	.	+	.	ID=3715;Variant_seq=T;Dbxref=dbSNP_129:rs18951442;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	265382	265382	.	+	.	ID=3716;Variant_seq=G;Dbxref=dbSNP_129:rs18951472;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	265624	265624	.	+	.	ID=3717;Variant_seq=C;Dbxref=dbSNP_129:rs18951542;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	266524	266524	.	+	.	ID=3718;Variant_seq=T;Dbxref=dbSNP_129:rs19590661;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	266804	266804	.	+	.	ID=3719;Variant_seq=C;Dbxref=dbSNP_129:rs19590651;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295498	295498	.	+	.	ID=3720;Variant_seq=T;Dbxref=dbSNP_129:rs53674159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295533	295533	.	+	.	ID=3721;Variant_seq=C;Dbxref=dbSNP_129:rs53272227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295538	295538	.	+	.	ID=3722;Variant_seq=T;Dbxref=dbSNP_129:rs54245298;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295540	295540	.	+	.	ID=3723;Variant_seq=C;Dbxref=dbSNP_129:rs53577718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295558	295558	.	+	.	ID=3724;Variant_seq=A;Dbxref=dbSNP_129:rs52967587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295564	295564	.	+	.	ID=3725;Variant_seq=C;Dbxref=dbSNP_129:rs54059880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	295567	295569	.	+	.	ID=3726;Variant_seq=-;Dbxref=dbSNP_129:rs54407693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=ATA
5	dbSNP	deletion	295574	295583	.	+	.	ID=3727;Variant_seq=-;Dbxref=dbSNP_129:rs53438030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=CCCAAATCCA
5	dbSNP	SNV	295589	295589	.	+	.	ID=3728;Variant_seq=A;Dbxref=dbSNP_129:rs53994498;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295598	295598	.	+	.	ID=3729;Variant_seq=G;Dbxref=dbSNP_129:rs53264695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295603	295603	.	+	.	ID=3730;Variant_seq=A;Dbxref=dbSNP_129:rs52901458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295605	295605	.	+	.	ID=3731;Variant_seq=A;Dbxref=dbSNP_129:rs54236863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295607	295607	.	+	.	ID=3732;Variant_seq=A;Dbxref=dbSNP_129:rs53387136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295614	295614	.	+	.	ID=3733;Variant_seq=G;Dbxref=dbSNP_129:rs53897598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295623	295623	.	+	.	ID=3734;Variant_seq=A;Dbxref=dbSNP_129:rs53033091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295627	295627	.	+	.	ID=3735;Variant_seq=C;Dbxref=dbSNP_129:rs52954293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295632	295632	.	+	.	ID=3736;Variant_seq=T;Dbxref=dbSNP_129:rs53197172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295650	295650	.	+	.	ID=3737;Variant_seq=T;Dbxref=dbSNP_129:rs53544084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295651	295651	.	+	.	ID=3738;Variant_seq=C;Dbxref=dbSNP_129:rs54010491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295655	295655	.	+	.	ID=3739;Variant_seq=T;Dbxref=dbSNP_129:rs53244158;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295662	295662	.	+	.	ID=3740;Variant_seq=A;Dbxref=dbSNP_129:rs53531426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295675	295675	.	+	.	ID=3741;Variant_seq=C;Dbxref=dbSNP_129:rs54333687;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	295682	295682	.	+	.	ID=3742;Variant_seq=-;Dbxref=dbSNP_129:rs54249517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295690	295690	.	+	.	ID=3743;Variant_seq=A;Dbxref=dbSNP_129:rs53122191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295691	295691	.	+	.	ID=3744;Variant_seq=G;Dbxref=dbSNP_129:rs53272104;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	295691	295691	.	+	.	ID=3745;Variant_seq=C;Dbxref=dbSNP_129:rs53969702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	295696	295696	.	+	.	ID=3746;Variant_seq=G;Dbxref=dbSNP_129:rs53350237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295705	295705	.	+	.	ID=3747;Variant_seq=G;Dbxref=dbSNP_129:rs53892901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295712	295712	.	+	.	ID=3748;Variant_seq=C;Dbxref=dbSNP_129:rs53282212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295718	295718	.	+	.	ID=3749;Variant_seq=G;Dbxref=dbSNP_129:rs53740169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295720	295720	.	+	.	ID=3750;Variant_seq=A;Dbxref=dbSNP_129:rs53319170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295727	295727	.	+	.	ID=3751;Variant_seq=G;Dbxref=dbSNP_129:rs53633532;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295738	295738	.	+	.	ID=3752;Variant_seq=G;Dbxref=dbSNP_129:rs54072547;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295758	295758	.	+	.	ID=3753;Variant_seq=G;Dbxref=dbSNP_129:rs53437663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295760	295760	.	+	.	ID=3754;Variant_seq=C;Dbxref=dbSNP_129:rs52994762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	295773	295773	.	+	.	ID=3755;Variant_seq=G;Dbxref=dbSNP_129:rs54143744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295774	295774	.	+	.	ID=3756;Variant_seq=T;Dbxref=dbSNP_129:rs53877513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295781	295781	.	+	.	ID=3757;Variant_seq=G;Dbxref=dbSNP_129:rs53417721;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295795	295795	.	+	.	ID=3758;Variant_seq=T;Dbxref=dbSNP_129:rs53439950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295796	295796	.	+	.	ID=3759;Variant_seq=G;Dbxref=dbSNP_129:rs53889815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295804	295804	.	+	.	ID=3760;Variant_seq=T;Dbxref=dbSNP_129:rs53200079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	deletion	295812	295814	.	+	.	ID=3761;Variant_seq=-;Dbxref=dbSNP_129:rs53710016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AAC
5	dbSNP	SNV	295843	295843	.	+	.	ID=3762;Variant_seq=A;Dbxref=dbSNP_129:rs52892277;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295850	295850	.	+	.	ID=3763;Variant_seq=C;Dbxref=dbSNP_129:rs53185780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295855	295855	.	+	.	ID=3764;Variant_seq=A;Dbxref=dbSNP_129:rs54034857;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	295858	295858	.	+	.	ID=3765;Variant_seq=T;Dbxref=dbSNP_129:rs53956555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	295864	295864	.	+	.	ID=3766;Variant_seq=T;Dbxref=dbSNP_129:rs53441100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	295867	295867	.	+	.	ID=3767;Variant_seq=C;Dbxref=dbSNP_129:rs53123583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	296911	296911	.	+	.	ID=3768;Variant_seq=T;Dbxref=dbSNP_129:rs53674159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	296946	296946	.	+	.	ID=3769;Variant_seq=C;Dbxref=dbSNP_129:rs53272227;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	296951	296951	.	+	.	ID=3770;Variant_seq=T;Dbxref=dbSNP_129:rs54245298;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	296953	296953	.	+	.	ID=3771;Variant_seq=C;Dbxref=dbSNP_129:rs53577718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	296971	296971	.	+	.	ID=3772;Variant_seq=A;Dbxref=dbSNP_129:rs52967587;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	296977	296977	.	+	.	ID=3773;Variant_seq=C;Dbxref=dbSNP_129:rs54059880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	296980	296982	.	+	.	ID=3774;Variant_seq=-;Dbxref=dbSNP_129:rs54407693;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=ATA
5	dbSNP	deletion	296987	296996	.	+	.	ID=3775;Variant_seq=-;Dbxref=dbSNP_129:rs53438030;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=CCCAAATCCA
5	dbSNP	SNV	297002	297002	.	+	.	ID=3776;Variant_seq=A;Dbxref=dbSNP_129:rs53994498;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297011	297011	.	+	.	ID=3777;Variant_seq=G;Dbxref=dbSNP_129:rs53264695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297016	297016	.	+	.	ID=3778;Variant_seq=A;Dbxref=dbSNP_129:rs52901458;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297018	297018	.	+	.	ID=3779;Variant_seq=A;Dbxref=dbSNP_129:rs54236863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297020	297020	.	+	.	ID=3780;Variant_seq=A;Dbxref=dbSNP_129:rs53387136;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297027	297027	.	+	.	ID=3781;Variant_seq=G;Dbxref=dbSNP_129:rs53897598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297036	297036	.	+	.	ID=3782;Variant_seq=A;Dbxref=dbSNP_129:rs53033091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297040	297040	.	+	.	ID=3783;Variant_seq=C;Dbxref=dbSNP_129:rs52954293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297045	297045	.	+	.	ID=3784;Variant_seq=T;Dbxref=dbSNP_129:rs53197172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297063	297063	.	+	.	ID=3785;Variant_seq=T;Dbxref=dbSNP_129:rs53544084;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297064	297064	.	+	.	ID=3786;Variant_seq=C;Dbxref=dbSNP_129:rs54010491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297068	297068	.	+	.	ID=3787;Variant_seq=T;Dbxref=dbSNP_129:rs53244158;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297075	297075	.	+	.	ID=3788;Variant_seq=A;Dbxref=dbSNP_129:rs53531426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297088	297088	.	+	.	ID=3789;Variant_seq=C;Dbxref=dbSNP_129:rs54333687;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	297095	297095	.	+	.	ID=3790;Variant_seq=-;Dbxref=dbSNP_129:rs54249517;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297103	297103	.	+	.	ID=3791;Variant_seq=A;Dbxref=dbSNP_129:rs53122191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297104	297104	.	+	.	ID=3792;Variant_seq=G;Dbxref=dbSNP_129:rs53272104;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	297104	297104	.	+	.	ID=3793;Variant_seq=C;Dbxref=dbSNP_129:rs53969702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	297109	297109	.	+	.	ID=3794;Variant_seq=G;Dbxref=dbSNP_129:rs53350237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297118	297118	.	+	.	ID=3795;Variant_seq=G;Dbxref=dbSNP_129:rs53892901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297125	297125	.	+	.	ID=3796;Variant_seq=C;Dbxref=dbSNP_129:rs53282212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297131	297131	.	+	.	ID=3797;Variant_seq=G;Dbxref=dbSNP_129:rs53740169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297133	297133	.	+	.	ID=3798;Variant_seq=A;Dbxref=dbSNP_129:rs53319170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297140	297140	.	+	.	ID=3799;Variant_seq=G;Dbxref=dbSNP_129:rs53633532;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297151	297151	.	+	.	ID=3800;Variant_seq=G;Dbxref=dbSNP_129:rs54072547;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297171	297171	.	+	.	ID=3801;Variant_seq=G;Dbxref=dbSNP_129:rs53437663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297173	297173	.	+	.	ID=3802;Variant_seq=C;Dbxref=dbSNP_129:rs52994762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	297186	297186	.	+	.	ID=3803;Variant_seq=G;Dbxref=dbSNP_129:rs54143744;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297187	297187	.	+	.	ID=3804;Variant_seq=T;Dbxref=dbSNP_129:rs53877513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297194	297194	.	+	.	ID=3805;Variant_seq=G;Dbxref=dbSNP_129:rs53417721;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297208	297208	.	+	.	ID=3806;Variant_seq=T;Dbxref=dbSNP_129:rs53439950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297209	297209	.	+	.	ID=3807;Variant_seq=G;Dbxref=dbSNP_129:rs53889815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297217	297217	.	+	.	ID=3808;Variant_seq=T;Dbxref=dbSNP_129:rs53200079;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	deletion	297225	297227	.	+	.	ID=3809;Variant_seq=-;Dbxref=dbSNP_129:rs53710016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AAC
5	dbSNP	SNV	297256	297256	.	+	.	ID=3810;Variant_seq=A;Dbxref=dbSNP_129:rs52892277;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297263	297263	.	+	.	ID=3811;Variant_seq=C;Dbxref=dbSNP_129:rs53185780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297268	297268	.	+	.	ID=3812;Variant_seq=A;Dbxref=dbSNP_129:rs54034857;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	297271	297271	.	+	.	ID=3813;Variant_seq=T;Dbxref=dbSNP_129:rs53956555;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	297277	297277	.	+	.	ID=3814;Variant_seq=T;Dbxref=dbSNP_129:rs53441100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	297280	297280	.	+	.	ID=3815;Variant_seq=C;Dbxref=dbSNP_129:rs53123583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313742	313742	.	+	.	ID=3816;Variant_seq=T;Dbxref=dbSNP_129:rs18961231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	313747	313747	.	+	.	ID=3817;Variant_seq=A;Dbxref=dbSNP_129:rs18961241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313750	313750	.	+	.	ID=3818;Variant_seq=G;Dbxref=dbSNP_129:rs18961251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313753	313753	.	+	.	ID=3819;Variant_seq=G;Dbxref=dbSNP_129:rs18961261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313756	313756	.	+	.	ID=3820;Variant_seq=C;Dbxref=dbSNP_129:rs18961271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313759	313759	.	+	.	ID=3821;Variant_seq=A;Dbxref=dbSNP_129:rs18961281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313760	313760	.	+	.	ID=3822;Variant_seq=A;Dbxref=dbSNP_129:rs18961291;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	313763	313763	.	+	.	ID=3823;Variant_seq=T;Dbxref=dbSNP_129:rs18961301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313766	313766	.	+	.	ID=3824;Variant_seq=T;Dbxref=dbSNP_129:rs18961311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313768	313768	.	+	.	ID=3825;Variant_seq=A;Dbxref=dbSNP_129:rs18961321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	313772	313772	.	+	.	ID=3826;Variant_seq=G;Dbxref=dbSNP_129:rs18961331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313773	313773	.	+	.	ID=3827;Variant_seq=T;Dbxref=dbSNP_129:rs18961341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313776	313776	.	+	.	ID=3828;Variant_seq=T;Dbxref=dbSNP_129:rs18961351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313778	313778	.	+	.	ID=3829;Variant_seq=T;Dbxref=dbSNP_129:rs18961361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313784	313784	.	+	.	ID=3830;Variant_seq=T;Dbxref=dbSNP_129:rs18961391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313785	313785	.	+	.	ID=3831;Variant_seq=C;Dbxref=dbSNP_129:rs18961401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313788	313788	.	+	.	ID=3832;Variant_seq=G;Dbxref=dbSNP_129:rs18961411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313790	313790	.	+	.	ID=3833;Variant_seq=C;Dbxref=dbSNP_129:rs18961421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313791	313791	.	+	.	ID=3834;Variant_seq=A;Dbxref=dbSNP_129:rs18961431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	313793	313793	.	+	.	ID=3835;Variant_seq=G;Dbxref=dbSNP_129:rs18961441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313797	313797	.	+	.	ID=3836;Variant_seq=T;Dbxref=dbSNP_129:rs18961451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313798	313798	.	+	.	ID=3837;Variant_seq=T;Dbxref=dbSNP_129:rs18961461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313803	313803	.	+	.	ID=3838;Variant_seq=C;Dbxref=dbSNP_129:rs18961471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313809	313809	.	+	.	ID=3839;Variant_seq=C;Dbxref=dbSNP_129:rs18961481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313816	313816	.	+	.	ID=3840;Variant_seq=C;Dbxref=dbSNP_129:rs18961491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313817	313817	.	+	.	ID=3841;Variant_seq=T;Dbxref=dbSNP_129:rs18961501;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313818	313818	.	+	.	ID=3842;Variant_seq=T;Dbxref=dbSNP_129:rs18961511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313826	313826	.	+	.	ID=3843;Variant_seq=A;Dbxref=dbSNP_129:rs18961541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313829	313829	.	+	.	ID=3844;Variant_seq=T;Dbxref=dbSNP_129:rs18961551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313833	313833	.	+	.	ID=3845;Variant_seq=A;Dbxref=dbSNP_129:rs18961561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313836	313836	.	+	.	ID=3846;Variant_seq=G;Dbxref=dbSNP_129:rs18961571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313842	313842	.	+	.	ID=3847;Variant_seq=G;Dbxref=dbSNP_129:rs18961581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	313844	313844	.	+	.	ID=3848;Variant_seq=T;Dbxref=dbSNP_129:rs18961601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313845	313845	.	+	.	ID=3849;Variant_seq=T;Dbxref=dbSNP_129:rs18961611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313852	313852	.	+	.	ID=3850;Variant_seq=T;Dbxref=dbSNP_129:rs18961621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	313913	313913	.	+	.	ID=3851;Variant_seq=A;Dbxref=dbSNP_129:rs18966999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313954	313954	.	+	.	ID=3852;Variant_seq=A;Dbxref=dbSNP_129:rs18967009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	313996	313996	.	+	.	ID=3853;Variant_seq=G;Dbxref=dbSNP_129:rs18962150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314005	314005	.	+	.	ID=3854;Variant_seq=T;Dbxref=dbSNP_129:rs18962170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314006	314006	.	+	.	ID=3855;Variant_seq=C;Dbxref=dbSNP_129:rs18962180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314008	314008	.	+	.	ID=3856;Variant_seq=C;Dbxref=dbSNP_129:rs18962190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314017	314017	.	+	.	ID=3857;Variant_seq=T;Dbxref=dbSNP_129:rs18962220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314020	314020	.	+	.	ID=3858;Variant_seq=C;Dbxref=dbSNP_129:rs18962230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314024	314024	.	+	.	ID=3859;Variant_seq=C;Dbxref=dbSNP_129:rs18962250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314042	314042	.	+	.	ID=3860;Variant_seq=T;Dbxref=dbSNP_129:rs18962283;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314043	314043	.	+	.	ID=3861;Variant_seq=T;Dbxref=dbSNP_129:rs18962293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314048	314048	.	+	.	ID=3862;Variant_seq=C;Dbxref=dbSNP_129:rs18962313;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314060	314060	.	+	.	ID=3863;Variant_seq=T;Dbxref=dbSNP_129:rs18962353;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314065	314065	.	+	.	ID=3864;Variant_seq=G;Dbxref=dbSNP_129:rs18962363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314066	314066	.	+	.	ID=3865;Variant_seq=G;Dbxref=dbSNP_129:rs18962373;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314072	314072	.	+	.	ID=3866;Variant_seq=C;Dbxref=dbSNP_129:rs18962393;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314073	314073	.	+	.	ID=3867;Variant_seq=G;Dbxref=dbSNP_129:rs18962403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314077	314077	.	+	.	ID=3868;Variant_seq=T;Dbxref=dbSNP_129:rs18962423;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314081	314081	.	+	.	ID=3869;Variant_seq=C;Dbxref=dbSNP_129:rs18962433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314090	314090	.	+	.	ID=3870;Variant_seq=G;Dbxref=dbSNP_129:rs18962463;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314091	314091	.	+	.	ID=3871;Variant_seq=A;Dbxref=dbSNP_129:rs18962473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314096	314096	.	+	.	ID=3872;Variant_seq=G;Dbxref=dbSNP_129:rs18962493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314098	314098	.	+	.	ID=3873;Variant_seq=C;Dbxref=dbSNP_129:rs18962503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314099	314099	.	+	.	ID=3874;Variant_seq=T;Dbxref=dbSNP_129:rs18962513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314101	314101	.	+	.	ID=3875;Variant_seq=G;Dbxref=dbSNP_129:rs18962533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314105	314105	.	+	.	ID=3876;Variant_seq=C;Dbxref=dbSNP_129:rs18962543;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314114	314114	.	+	.	ID=3877;Variant_seq=A;Dbxref=dbSNP_129:rs18962583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314118	314118	.	+	.	ID=3878;Variant_seq=A;Dbxref=dbSNP_129:rs18962593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314120	314120	.	+	.	ID=3879;Variant_seq=A;Dbxref=dbSNP_129:rs18962613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314132	314132	.	+	.	ID=3880;Variant_seq=A;Dbxref=dbSNP_129:rs18962643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314138	314138	.	+	.	ID=3881;Variant_seq=T;Dbxref=dbSNP_129:rs18962663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314139	314139	.	+	.	ID=3882;Variant_seq=G;Dbxref=dbSNP_129:rs18962673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314140	314140	.	+	.	ID=3883;Variant_seq=G;Dbxref=dbSNP_129:rs18962683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314144	314144	.	+	.	ID=3884;Variant_seq=C;Dbxref=dbSNP_129:rs18962713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314146	314146	.	+	.	ID=3885;Variant_seq=G;Dbxref=dbSNP_129:rs18962723;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314149	314149	.	+	.	ID=3886;Variant_seq=G;Dbxref=dbSNP_129:rs18962743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314150	314150	.	+	.	ID=3887;Variant_seq=T;Dbxref=dbSNP_129:rs18962753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314152	314152	.	+	.	ID=3888;Variant_seq=G;Dbxref=dbSNP_129:rs18962763;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314153	314153	.	+	.	ID=3889;Variant_seq=G;Dbxref=dbSNP_129:rs18962773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314156	314156	.	+	.	ID=3890;Variant_seq=C;Dbxref=dbSNP_129:rs18962783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314157	314157	.	+	.	ID=3891;Variant_seq=C;Dbxref=dbSNP_129:rs18962793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314164	314164	.	+	.	ID=3892;Variant_seq=C;Dbxref=dbSNP_129:rs18962813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314168	314168	.	+	.	ID=3893;Variant_seq=C;Dbxref=dbSNP_129:rs18962833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314176	314176	.	+	.	ID=3894;Variant_seq=T;Dbxref=dbSNP_129:rs18962863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314177	314177	.	+	.	ID=3895;Variant_seq=C;Dbxref=dbSNP_129:rs18962873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314180	314180	.	+	.	ID=3896;Variant_seq=C;Dbxref=dbSNP_129:rs18962893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314181	314181	.	+	.	ID=3897;Variant_seq=C;Dbxref=dbSNP_129:rs18962903;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314193	314193	.	+	.	ID=3898;Variant_seq=T;Dbxref=dbSNP_129:rs18962913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314197	314197	.	+	.	ID=3899;Variant_seq=C;Dbxref=dbSNP_129:rs18962932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314199	314199	.	+	.	ID=3900;Variant_seq=C;Dbxref=dbSNP_129:rs18962942;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314200	314200	.	+	.	ID=3901;Variant_seq=C;Dbxref=dbSNP_129:rs18962952;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314205	314205	.	+	.	ID=3902;Variant_seq=C;Dbxref=dbSNP_129:rs18962972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314206	314206	.	+	.	ID=3903;Variant_seq=C;Dbxref=dbSNP_129:rs18962982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314209	314209	.	+	.	ID=3904;Variant_seq=C;Dbxref=dbSNP_129:rs18963012;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314210	314210	.	+	.	ID=3905;Variant_seq=A;Dbxref=dbSNP_129:rs18963022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314217	314217	.	+	.	ID=3906;Variant_seq=G;Dbxref=dbSNP_129:rs18963042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314221	314221	.	+	.	ID=3907;Variant_seq=A;Dbxref=dbSNP_129:rs18963052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314222	314222	.	+	.	ID=3908;Variant_seq=C;Dbxref=dbSNP_129:rs18963062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314224	314224	.	+	.	ID=3909;Variant_seq=C;Dbxref=dbSNP_129:rs18963072;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314227	314227	.	+	.	ID=3910;Variant_seq=A;Dbxref=dbSNP_129:rs18963082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314230	314230	.	+	.	ID=3911;Variant_seq=T;Dbxref=dbSNP_129:rs18963092;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314234	314234	.	+	.	ID=3912;Variant_seq=A;Dbxref=dbSNP_129:rs18963112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314237	314237	.	+	.	ID=3913;Variant_seq=T;Dbxref=dbSNP_129:rs18963122;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314240	314240	.	+	.	ID=3914;Variant_seq=T;Dbxref=dbSNP_129:rs18963152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314245	314245	.	+	.	ID=3915;Variant_seq=T;Dbxref=dbSNP_129:rs18963182;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314247	314247	.	+	.	ID=3916;Variant_seq=T;Dbxref=dbSNP_129:rs18963192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314252	314252	.	+	.	ID=3917;Variant_seq=G;Dbxref=dbSNP_129:rs18963212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314260	314260	.	+	.	ID=3918;Variant_seq=G;Dbxref=dbSNP_129:rs18963232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314261	314261	.	+	.	ID=3919;Variant_seq=A;Dbxref=dbSNP_129:rs18963242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314262	314262	.	+	.	ID=3920;Variant_seq=A;Dbxref=dbSNP_129:rs18963252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314263	314263	.	+	.	ID=3921;Variant_seq=A;Dbxref=dbSNP_129:rs18963262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314265	314265	.	+	.	ID=3922;Variant_seq=G;Dbxref=dbSNP_129:rs18963272;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314266	314266	.	+	.	ID=3923;Variant_seq=T;Dbxref=dbSNP_129:rs18963282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314270	314270	.	+	.	ID=3924;Variant_seq=T;Dbxref=dbSNP_129:rs18963302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314271	314271	.	+	.	ID=3925;Variant_seq=T;Dbxref=dbSNP_129:rs18963312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314278	314278	.	+	.	ID=3926;Variant_seq=T;Dbxref=dbSNP_129:rs18963331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314282	314282	.	+	.	ID=3927;Variant_seq=T;Dbxref=dbSNP_129:rs18963351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314283	314283	.	+	.	ID=3928;Variant_seq=T;Dbxref=dbSNP_129:rs18963361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314289	314289	.	+	.	ID=3929;Variant_seq=C;Dbxref=dbSNP_129:rs18963391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314296	314296	.	+	.	ID=3930;Variant_seq=G;Dbxref=dbSNP_129:rs18963401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314297	314297	.	+	.	ID=3931;Variant_seq=T;Dbxref=dbSNP_129:rs18963411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314300	314300	.	+	.	ID=3932;Variant_seq=C;Dbxref=dbSNP_129:rs18963421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314301	314301	.	+	.	ID=3933;Variant_seq=A;Dbxref=dbSNP_129:rs18963431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314302	314302	.	+	.	ID=3934;Variant_seq=A;Dbxref=dbSNP_129:rs18963441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314307	314307	.	+	.	ID=3935;Variant_seq=A;Dbxref=dbSNP_129:rs18963451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314309	314309	.	+	.	ID=3936;Variant_seq=A;Dbxref=dbSNP_129:rs18963461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314312	314312	.	+	.	ID=3937;Variant_seq=T;Dbxref=dbSNP_129:rs18963471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314313	314313	.	+	.	ID=3938;Variant_seq=T;Dbxref=dbSNP_129:rs18963481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314314	314314	.	+	.	ID=3939;Variant_seq=T;Dbxref=dbSNP_129:rs18963491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314320	314320	.	+	.	ID=3940;Variant_seq=G;Dbxref=dbSNP_129:rs18963521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314325	314325	.	+	.	ID=3941;Variant_seq=G;Dbxref=dbSNP_129:rs18963531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314329	314329	.	+	.	ID=3942;Variant_seq=C;Dbxref=dbSNP_129:rs18963551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314330	314330	.	+	.	ID=3943;Variant_seq=C;Dbxref=dbSNP_129:rs18963561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314338	314338	.	+	.	ID=3944;Variant_seq=G;Dbxref=dbSNP_129:rs18963571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314341	314341	.	+	.	ID=3945;Variant_seq=T;Dbxref=dbSNP_129:rs18963593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314342	314342	.	+	.	ID=3946;Variant_seq=G;Dbxref=dbSNP_129:rs18963603;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314343	314343	.	+	.	ID=3947;Variant_seq=C;Dbxref=dbSNP_129:rs18963613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314424	314424	.	+	.	ID=3948;Variant_seq=A;Dbxref=dbSNP_129:rs18963923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314425	314425	.	+	.	ID=3949;Variant_seq=T;Dbxref=dbSNP_129:rs18963933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314428	314428	.	+	.	ID=3950;Variant_seq=A;Dbxref=dbSNP_129:rs18963943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314432	314432	.	+	.	ID=3951;Variant_seq=C;Dbxref=dbSNP_129:rs18963953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314433	314433	.	+	.	ID=3952;Variant_seq=A;Dbxref=dbSNP_129:rs18963963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314437	314437	.	+	.	ID=3953;Variant_seq=T;Dbxref=dbSNP_129:rs18963982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314444	314444	.	+	.	ID=3954;Variant_seq=C;Dbxref=dbSNP_129:rs18964002;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314449	314449	.	+	.	ID=3955;Variant_seq=C;Dbxref=dbSNP_129:rs18964032;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314450	314450	.	+	.	ID=3956;Variant_seq=A;Dbxref=dbSNP_129:rs18964042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314455	314455	.	+	.	ID=3957;Variant_seq=G;Dbxref=dbSNP_129:rs18964052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314456	314456	.	+	.	ID=3958;Variant_seq=G;Dbxref=dbSNP_129:rs18964062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314460	314460	.	+	.	ID=3959;Variant_seq=G;Dbxref=dbSNP_129:rs18964081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314461	314461	.	+	.	ID=3960;Variant_seq=C;Dbxref=dbSNP_129:rs18964091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314463	314463	.	+	.	ID=3961;Variant_seq=T;Dbxref=dbSNP_129:rs18964101;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314464	314464	.	+	.	ID=3962;Variant_seq=T;Dbxref=dbSNP_129:rs18964111;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314465	314465	.	+	.	ID=3963;Variant_seq=T;Dbxref=dbSNP_129:rs18964121;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314468	314468	.	+	.	ID=3964;Variant_seq=G;Dbxref=dbSNP_129:rs18964141;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314473	314473	.	+	.	ID=3965;Variant_seq=A;Dbxref=dbSNP_129:rs18964161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314474	314474	.	+	.	ID=3966;Variant_seq=A;Dbxref=dbSNP_129:rs18964171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314475	314475	.	+	.	ID=3967;Variant_seq=G;Dbxref=dbSNP_129:rs18964181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314478	314478	.	+	.	ID=3968;Variant_seq=G;Dbxref=dbSNP_129:rs18964191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314485	314485	.	+	.	ID=3969;Variant_seq=T;Dbxref=dbSNP_129:rs18964201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314486	314486	.	+	.	ID=3970;Variant_seq=C;Dbxref=dbSNP_129:rs18964211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314488	314488	.	+	.	ID=3971;Variant_seq=A;Dbxref=dbSNP_129:rs18964221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314492	314492	.	+	.	ID=3972;Variant_seq=A;Dbxref=dbSNP_129:rs18964231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314496	314496	.	+	.	ID=3973;Variant_seq=C;Dbxref=dbSNP_129:rs18964251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314500	314500	.	+	.	ID=3974;Variant_seq=G;Dbxref=dbSNP_129:rs18964261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314511	314511	.	+	.	ID=3975;Variant_seq=C;Dbxref=dbSNP_129:rs18964271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314516	314516	.	+	.	ID=3976;Variant_seq=C;Dbxref=dbSNP_129:rs18964281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314521	314521	.	+	.	ID=3977;Variant_seq=T;Dbxref=dbSNP_129:rs18964301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314522	314522	.	+	.	ID=3978;Variant_seq=C;Dbxref=dbSNP_129:rs18964311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314523	314523	.	+	.	ID=3979;Variant_seq=C;Dbxref=dbSNP_129:rs18964321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314705	314705	.	+	.	ID=3980;Variant_seq=G;Dbxref=dbSNP_129:rs18964861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314708	314708	.	+	.	ID=3981;Variant_seq=C;Dbxref=dbSNP_129:rs18964871;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314710	314710	.	+	.	ID=3982;Variant_seq=C;Dbxref=dbSNP_129:rs18964881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314711	314711	.	+	.	ID=3983;Variant_seq=T;Dbxref=dbSNP_129:rs18964891;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314712	314712	.	+	.	ID=3984;Variant_seq=A;Dbxref=dbSNP_129:rs18964901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314714	314714	.	+	.	ID=3985;Variant_seq=G;Dbxref=dbSNP_129:rs18964911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314717	314717	.	+	.	ID=3986;Variant_seq=C;Dbxref=dbSNP_129:rs18964921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314792	314792	.	+	.	ID=3987;Variant_seq=T;Dbxref=dbSNP_129:rs18965151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314793	314793	.	+	.	ID=3988;Variant_seq=C;Dbxref=dbSNP_129:rs18965161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314794	314794	.	+	.	ID=3989;Variant_seq=T;Dbxref=dbSNP_129:rs18965171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314795	314795	.	+	.	ID=3990;Variant_seq=C;Dbxref=dbSNP_129:rs18965181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314799	314799	.	+	.	ID=3991;Variant_seq=C;Dbxref=dbSNP_129:rs18965191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314805	314805	.	+	.	ID=3992;Variant_seq=G;Dbxref=dbSNP_129:rs18965211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314811	314811	.	+	.	ID=3993;Variant_seq=C;Dbxref=dbSNP_129:rs18965221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314812	314812	.	+	.	ID=3994;Variant_seq=G;Dbxref=dbSNP_129:rs18965231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314817	314817	.	+	.	ID=3995;Variant_seq=T;Dbxref=dbSNP_129:rs18965241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314823	314823	.	+	.	ID=3996;Variant_seq=C;Dbxref=dbSNP_129:rs18965251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314828	314828	.	+	.	ID=3997;Variant_seq=C;Dbxref=dbSNP_129:rs18965291;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314831	314831	.	+	.	ID=3998;Variant_seq=T;Dbxref=dbSNP_129:rs18965301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314832	314832	.	+	.	ID=3999;Variant_seq=G;Dbxref=dbSNP_129:rs18965311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314833	314833	.	+	.	ID=4000;Variant_seq=C;Dbxref=dbSNP_129:rs18965321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314835	314835	.	+	.	ID=4001;Variant_seq=G;Dbxref=dbSNP_129:rs18965331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314840	314840	.	+	.	ID=4002;Variant_seq=A;Dbxref=dbSNP_129:rs18965351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314843	314843	.	+	.	ID=4003;Variant_seq=A;Dbxref=dbSNP_129:rs18965361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314844	314844	.	+	.	ID=4004;Variant_seq=A;Dbxref=dbSNP_129:rs18965371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314847	314847	.	+	.	ID=4005;Variant_seq=T;Dbxref=dbSNP_129:rs18965381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314851	314851	.	+	.	ID=4006;Variant_seq=T;Dbxref=dbSNP_129:rs18965391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314854	314854	.	+	.	ID=4007;Variant_seq=A;Dbxref=dbSNP_129:rs18965401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	314855	314855	.	+	.	ID=4008;Variant_seq=T;Dbxref=dbSNP_129:rs18965411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314856	314856	.	+	.	ID=4009;Variant_seq=T;Dbxref=dbSNP_129:rs18965421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314935	314935	.	+	.	ID=4010;Variant_seq=G;Dbxref=dbSNP_129:rs18965761;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314936	314936	.	+	.	ID=4011;Variant_seq=G;Dbxref=dbSNP_129:rs18965771;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314943	314943	.	+	.	ID=4012;Variant_seq=T;Dbxref=dbSNP_129:rs18965781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314945	314945	.	+	.	ID=4013;Variant_seq=G;Dbxref=dbSNP_129:rs18965791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314948	314948	.	+	.	ID=4014;Variant_seq=T;Dbxref=dbSNP_129:rs18965811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314950	314950	.	+	.	ID=4015;Variant_seq=C;Dbxref=dbSNP_129:rs18965821;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314957	314957	.	+	.	ID=4016;Variant_seq=A;Dbxref=dbSNP_129:rs18965840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314963	314963	.	+	.	ID=4017;Variant_seq=A;Dbxref=dbSNP_129:rs18965850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314966	314966	.	+	.	ID=4018;Variant_seq=C;Dbxref=dbSNP_129:rs18965860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314990	314990	.	+	.	ID=4019;Variant_seq=A;Dbxref=dbSNP_129:rs18965880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314992	314992	.	+	.	ID=4020;Variant_seq=T;Dbxref=dbSNP_129:rs18965890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	314993	314993	.	+	.	ID=4021;Variant_seq=T;Dbxref=dbSNP_129:rs18965900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	314996	314996	.	+	.	ID=4022;Variant_seq=T;Dbxref=dbSNP_129:rs18965910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	314999	314999	.	+	.	ID=4023;Variant_seq=T;Dbxref=dbSNP_129:rs18965920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	315003	315003	.	+	.	ID=4024;Variant_seq=T;Dbxref=dbSNP_129:rs18965950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315004	315004	.	+	.	ID=4025;Variant_seq=A;Dbxref=dbSNP_129:rs18965960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	315005	315005	.	+	.	ID=4026;Variant_seq=A;Dbxref=dbSNP_129:rs18965970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	315466	315466	.	+	.	ID=4027;Variant_seq=C;Dbxref=dbSNP_129:rs18967019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	315541	315541	.	+	.	ID=4028;Variant_seq=C;Dbxref=dbSNP_129:rs18966140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315544	315544	.	+	.	ID=4029;Variant_seq=C;Dbxref=dbSNP_129:rs18966160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315545	315545	.	+	.	ID=4030;Variant_seq=C;Dbxref=dbSNP_129:rs18966170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315548	315548	.	+	.	ID=4031;Variant_seq=C;Dbxref=dbSNP_129:rs18966190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315550	315550	.	+	.	ID=4032;Variant_seq=A;Dbxref=dbSNP_129:rs18966200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315551	315551	.	+	.	ID=4033;Variant_seq=A;Dbxref=dbSNP_129:rs18966210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315552	315552	.	+	.	ID=4034;Variant_seq=T;Dbxref=dbSNP_129:rs18966220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315554	315554	.	+	.	ID=4035;Variant_seq=G;Dbxref=dbSNP_129:rs18966230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	315556	315556	.	+	.	ID=4036;Variant_seq=T;Dbxref=dbSNP_129:rs18966250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	315557	315557	.	+	.	ID=4037;Variant_seq=T;Dbxref=dbSNP_129:rs18966260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315560	315560	.	+	.	ID=4038;Variant_seq=T;Dbxref=dbSNP_129:rs18966290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315561	315561	.	+	.	ID=4039;Variant_seq=C;Dbxref=dbSNP_129:rs18966300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315562	315562	.	+	.	ID=4040;Variant_seq=T;Dbxref=dbSNP_129:rs18966310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	315564	315564	.	+	.	ID=4041;Variant_seq=T;Dbxref=dbSNP_129:rs18966320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315574	315574	.	+	.	ID=4042;Variant_seq=C;Dbxref=dbSNP_129:rs18966340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315575	315575	.	+	.	ID=4043;Variant_seq=A;Dbxref=dbSNP_129:rs18966350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	315580	315580	.	+	.	ID=4044;Variant_seq=G;Dbxref=dbSNP_129:rs18966370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	315582	315582	.	+	.	ID=4045;Variant_seq=T;Dbxref=dbSNP_129:rs18966380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	315694	315694	.	+	.	ID=4046;Variant_seq=A;Dbxref=dbSNP_129:rs18966709;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	315695	315695	.	+	.	ID=4047;Variant_seq=A;Dbxref=dbSNP_129:rs18966719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	315696	315696	.	+	.	ID=4048;Variant_seq=A;Dbxref=dbSNP_129:rs18966729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	315699	315699	.	+	.	ID=4049;Variant_seq=A;Dbxref=dbSNP_129:rs18966739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317085	317085	.	+	.	ID=4050;Variant_seq=T;Dbxref=dbSNP_129:rs18961231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317090	317090	.	+	.	ID=4051;Variant_seq=A;Dbxref=dbSNP_129:rs18961241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317093	317093	.	+	.	ID=4052;Variant_seq=G;Dbxref=dbSNP_129:rs18961251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317096	317096	.	+	.	ID=4053;Variant_seq=G;Dbxref=dbSNP_129:rs18961261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317099	317099	.	+	.	ID=4054;Variant_seq=C;Dbxref=dbSNP_129:rs18961271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317102	317102	.	+	.	ID=4055;Variant_seq=A;Dbxref=dbSNP_129:rs18961281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317103	317103	.	+	.	ID=4056;Variant_seq=A;Dbxref=dbSNP_129:rs18961291;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317106	317106	.	+	.	ID=4057;Variant_seq=T;Dbxref=dbSNP_129:rs18961301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317109	317109	.	+	.	ID=4058;Variant_seq=T;Dbxref=dbSNP_129:rs18961311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317111	317111	.	+	.	ID=4059;Variant_seq=A;Dbxref=dbSNP_129:rs18961321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317115	317115	.	+	.	ID=4060;Variant_seq=G;Dbxref=dbSNP_129:rs18961331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317116	317116	.	+	.	ID=4061;Variant_seq=T;Dbxref=dbSNP_129:rs18961341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317119	317119	.	+	.	ID=4062;Variant_seq=T;Dbxref=dbSNP_129:rs18961351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317121	317121	.	+	.	ID=4063;Variant_seq=T;Dbxref=dbSNP_129:rs18961361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317127	317127	.	+	.	ID=4064;Variant_seq=T;Dbxref=dbSNP_129:rs18961391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317128	317128	.	+	.	ID=4065;Variant_seq=C;Dbxref=dbSNP_129:rs18961401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317131	317131	.	+	.	ID=4066;Variant_seq=G;Dbxref=dbSNP_129:rs18961411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317133	317133	.	+	.	ID=4067;Variant_seq=C;Dbxref=dbSNP_129:rs18961421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317134	317134	.	+	.	ID=4068;Variant_seq=A;Dbxref=dbSNP_129:rs18961431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317136	317136	.	+	.	ID=4069;Variant_seq=G;Dbxref=dbSNP_129:rs18961441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317140	317140	.	+	.	ID=4070;Variant_seq=T;Dbxref=dbSNP_129:rs18961451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317141	317141	.	+	.	ID=4071;Variant_seq=T;Dbxref=dbSNP_129:rs18961461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317146	317146	.	+	.	ID=4072;Variant_seq=C;Dbxref=dbSNP_129:rs18961471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317152	317152	.	+	.	ID=4073;Variant_seq=C;Dbxref=dbSNP_129:rs18961481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317159	317159	.	+	.	ID=4074;Variant_seq=C;Dbxref=dbSNP_129:rs18961491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317160	317160	.	+	.	ID=4075;Variant_seq=T;Dbxref=dbSNP_129:rs18961501;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317161	317161	.	+	.	ID=4076;Variant_seq=T;Dbxref=dbSNP_129:rs18961511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317169	317169	.	+	.	ID=4077;Variant_seq=A;Dbxref=dbSNP_129:rs18961541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317172	317172	.	+	.	ID=4078;Variant_seq=T;Dbxref=dbSNP_129:rs18961551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317176	317176	.	+	.	ID=4079;Variant_seq=A;Dbxref=dbSNP_129:rs18961561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317179	317179	.	+	.	ID=4080;Variant_seq=G;Dbxref=dbSNP_129:rs18961571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317185	317185	.	+	.	ID=4081;Variant_seq=G;Dbxref=dbSNP_129:rs18961581;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317187	317187	.	+	.	ID=4082;Variant_seq=T;Dbxref=dbSNP_129:rs18961601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317188	317188	.	+	.	ID=4083;Variant_seq=T;Dbxref=dbSNP_129:rs18961611;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317195	317195	.	+	.	ID=4084;Variant_seq=T;Dbxref=dbSNP_129:rs18961621;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317256	317256	.	+	.	ID=4085;Variant_seq=T;Dbxref=dbSNP_129:rs18966999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317297	317297	.	+	.	ID=4086;Variant_seq=T;Dbxref=dbSNP_129:rs18967009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317339	317339	.	+	.	ID=4087;Variant_seq=G;Dbxref=dbSNP_129:rs18962150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317348	317348	.	+	.	ID=4088;Variant_seq=T;Dbxref=dbSNP_129:rs18962170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317349	317349	.	+	.	ID=4089;Variant_seq=C;Dbxref=dbSNP_129:rs18962180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317351	317351	.	+	.	ID=4090;Variant_seq=C;Dbxref=dbSNP_129:rs18962190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317360	317360	.	+	.	ID=4091;Variant_seq=T;Dbxref=dbSNP_129:rs18962220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317363	317363	.	+	.	ID=4092;Variant_seq=C;Dbxref=dbSNP_129:rs18962230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317367	317367	.	+	.	ID=4093;Variant_seq=C;Dbxref=dbSNP_129:rs18962250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317385	317385	.	+	.	ID=4094;Variant_seq=T;Dbxref=dbSNP_129:rs18962283;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317386	317386	.	+	.	ID=4095;Variant_seq=T;Dbxref=dbSNP_129:rs18962293;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317391	317391	.	+	.	ID=4096;Variant_seq=C;Dbxref=dbSNP_129:rs18962313;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317403	317403	.	+	.	ID=4097;Variant_seq=T;Dbxref=dbSNP_129:rs18962353;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317408	317408	.	+	.	ID=4098;Variant_seq=G;Dbxref=dbSNP_129:rs18962363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317409	317409	.	+	.	ID=4099;Variant_seq=G;Dbxref=dbSNP_129:rs18962373;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317415	317415	.	+	.	ID=4100;Variant_seq=C;Dbxref=dbSNP_129:rs18962393;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317416	317416	.	+	.	ID=4101;Variant_seq=G;Dbxref=dbSNP_129:rs18962403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317420	317420	.	+	.	ID=4102;Variant_seq=T;Dbxref=dbSNP_129:rs18962423;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317424	317424	.	+	.	ID=4103;Variant_seq=C;Dbxref=dbSNP_129:rs18962433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317433	317433	.	+	.	ID=4104;Variant_seq=G;Dbxref=dbSNP_129:rs18962463;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317434	317434	.	+	.	ID=4105;Variant_seq=A;Dbxref=dbSNP_129:rs18962473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317439	317439	.	+	.	ID=4106;Variant_seq=G;Dbxref=dbSNP_129:rs18962493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317441	317441	.	+	.	ID=4107;Variant_seq=C;Dbxref=dbSNP_129:rs18962503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317442	317442	.	+	.	ID=4108;Variant_seq=T;Dbxref=dbSNP_129:rs18962513;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317444	317444	.	+	.	ID=4109;Variant_seq=G;Dbxref=dbSNP_129:rs18962533;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317448	317448	.	+	.	ID=4110;Variant_seq=C;Dbxref=dbSNP_129:rs18962543;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317457	317457	.	+	.	ID=4111;Variant_seq=A;Dbxref=dbSNP_129:rs18962583;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317461	317461	.	+	.	ID=4112;Variant_seq=A;Dbxref=dbSNP_129:rs18962593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317463	317463	.	+	.	ID=4113;Variant_seq=A;Dbxref=dbSNP_129:rs18962613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317475	317475	.	+	.	ID=4114;Variant_seq=A;Dbxref=dbSNP_129:rs18962643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317481	317481	.	+	.	ID=4115;Variant_seq=T;Dbxref=dbSNP_129:rs18962663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317482	317482	.	+	.	ID=4116;Variant_seq=G;Dbxref=dbSNP_129:rs18962673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317483	317483	.	+	.	ID=4117;Variant_seq=G;Dbxref=dbSNP_129:rs18962683;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317487	317487	.	+	.	ID=4118;Variant_seq=C;Dbxref=dbSNP_129:rs18962713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317489	317489	.	+	.	ID=4119;Variant_seq=G;Dbxref=dbSNP_129:rs18962723;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317492	317492	.	+	.	ID=4120;Variant_seq=G;Dbxref=dbSNP_129:rs18962743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317493	317493	.	+	.	ID=4121;Variant_seq=T;Dbxref=dbSNP_129:rs18962753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317495	317495	.	+	.	ID=4122;Variant_seq=G;Dbxref=dbSNP_129:rs18962763;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317496	317496	.	+	.	ID=4123;Variant_seq=G;Dbxref=dbSNP_129:rs18962773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317499	317499	.	+	.	ID=4124;Variant_seq=C;Dbxref=dbSNP_129:rs18962783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317500	317500	.	+	.	ID=4125;Variant_seq=C;Dbxref=dbSNP_129:rs18962793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317507	317507	.	+	.	ID=4126;Variant_seq=C;Dbxref=dbSNP_129:rs18962813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317511	317511	.	+	.	ID=4127;Variant_seq=C;Dbxref=dbSNP_129:rs18962833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317519	317519	.	+	.	ID=4128;Variant_seq=T;Dbxref=dbSNP_129:rs18962863;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317520	317520	.	+	.	ID=4129;Variant_seq=C;Dbxref=dbSNP_129:rs18962873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317523	317523	.	+	.	ID=4130;Variant_seq=C;Dbxref=dbSNP_129:rs18962893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317524	317524	.	+	.	ID=4131;Variant_seq=C;Dbxref=dbSNP_129:rs18962903;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317536	317536	.	+	.	ID=4132;Variant_seq=T;Dbxref=dbSNP_129:rs18962913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317540	317540	.	+	.	ID=4133;Variant_seq=C;Dbxref=dbSNP_129:rs18962932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317542	317542	.	+	.	ID=4134;Variant_seq=C;Dbxref=dbSNP_129:rs18962942;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317543	317543	.	+	.	ID=4135;Variant_seq=C;Dbxref=dbSNP_129:rs18962952;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317548	317548	.	+	.	ID=4136;Variant_seq=C;Dbxref=dbSNP_129:rs18962972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317549	317549	.	+	.	ID=4137;Variant_seq=C;Dbxref=dbSNP_129:rs18962982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317552	317552	.	+	.	ID=4138;Variant_seq=C;Dbxref=dbSNP_129:rs18963012;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317553	317553	.	+	.	ID=4139;Variant_seq=A;Dbxref=dbSNP_129:rs18963022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317560	317560	.	+	.	ID=4140;Variant_seq=G;Dbxref=dbSNP_129:rs18963042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317564	317564	.	+	.	ID=4141;Variant_seq=A;Dbxref=dbSNP_129:rs18963052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317565	317565	.	+	.	ID=4142;Variant_seq=C;Dbxref=dbSNP_129:rs18963062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317567	317567	.	+	.	ID=4143;Variant_seq=C;Dbxref=dbSNP_129:rs18963072;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317570	317570	.	+	.	ID=4144;Variant_seq=A;Dbxref=dbSNP_129:rs18963082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317573	317573	.	+	.	ID=4145;Variant_seq=T;Dbxref=dbSNP_129:rs18963092;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317577	317577	.	+	.	ID=4146;Variant_seq=A;Dbxref=dbSNP_129:rs18963112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317580	317580	.	+	.	ID=4147;Variant_seq=T;Dbxref=dbSNP_129:rs18963122;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317583	317583	.	+	.	ID=4148;Variant_seq=T;Dbxref=dbSNP_129:rs18963152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317588	317588	.	+	.	ID=4149;Variant_seq=T;Dbxref=dbSNP_129:rs18963182;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317590	317590	.	+	.	ID=4150;Variant_seq=T;Dbxref=dbSNP_129:rs18963192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317595	317595	.	+	.	ID=4151;Variant_seq=G;Dbxref=dbSNP_129:rs18963212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317603	317603	.	+	.	ID=4152;Variant_seq=G;Dbxref=dbSNP_129:rs18963232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317604	317604	.	+	.	ID=4153;Variant_seq=A;Dbxref=dbSNP_129:rs18963242;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317605	317605	.	+	.	ID=4154;Variant_seq=A;Dbxref=dbSNP_129:rs18963252;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317606	317606	.	+	.	ID=4155;Variant_seq=A;Dbxref=dbSNP_129:rs18963262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317608	317608	.	+	.	ID=4156;Variant_seq=G;Dbxref=dbSNP_129:rs18963272;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317609	317609	.	+	.	ID=4157;Variant_seq=T;Dbxref=dbSNP_129:rs18963282;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317613	317613	.	+	.	ID=4158;Variant_seq=T;Dbxref=dbSNP_129:rs18963302;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317614	317614	.	+	.	ID=4159;Variant_seq=T;Dbxref=dbSNP_129:rs18963312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317621	317621	.	+	.	ID=4160;Variant_seq=T;Dbxref=dbSNP_129:rs18963331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317625	317625	.	+	.	ID=4161;Variant_seq=T;Dbxref=dbSNP_129:rs18963351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317626	317626	.	+	.	ID=4162;Variant_seq=T;Dbxref=dbSNP_129:rs18963361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317632	317632	.	+	.	ID=4163;Variant_seq=C;Dbxref=dbSNP_129:rs18963391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317639	317639	.	+	.	ID=4164;Variant_seq=G;Dbxref=dbSNP_129:rs18963401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317640	317640	.	+	.	ID=4165;Variant_seq=T;Dbxref=dbSNP_129:rs18963411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317643	317643	.	+	.	ID=4166;Variant_seq=C;Dbxref=dbSNP_129:rs18963421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317644	317644	.	+	.	ID=4167;Variant_seq=A;Dbxref=dbSNP_129:rs18963431;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317645	317645	.	+	.	ID=4168;Variant_seq=A;Dbxref=dbSNP_129:rs18963441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317650	317650	.	+	.	ID=4169;Variant_seq=A;Dbxref=dbSNP_129:rs18963451;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317652	317652	.	+	.	ID=4170;Variant_seq=A;Dbxref=dbSNP_129:rs18963461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317655	317655	.	+	.	ID=4171;Variant_seq=T;Dbxref=dbSNP_129:rs18963471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317656	317656	.	+	.	ID=4172;Variant_seq=T;Dbxref=dbSNP_129:rs18963481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317657	317657	.	+	.	ID=4173;Variant_seq=T;Dbxref=dbSNP_129:rs18963491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317663	317663	.	+	.	ID=4174;Variant_seq=G;Dbxref=dbSNP_129:rs18963521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317668	317668	.	+	.	ID=4175;Variant_seq=G;Dbxref=dbSNP_129:rs18963531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317672	317672	.	+	.	ID=4176;Variant_seq=C;Dbxref=dbSNP_129:rs18963551;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317673	317673	.	+	.	ID=4177;Variant_seq=C;Dbxref=dbSNP_129:rs18963561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317681	317681	.	+	.	ID=4178;Variant_seq=G;Dbxref=dbSNP_129:rs18963571;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317684	317684	.	+	.	ID=4179;Variant_seq=T;Dbxref=dbSNP_129:rs18963593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317685	317685	.	+	.	ID=4180;Variant_seq=G;Dbxref=dbSNP_129:rs18963603;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317686	317686	.	+	.	ID=4181;Variant_seq=C;Dbxref=dbSNP_129:rs18963613;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317768	317768	.	+	.	ID=4182;Variant_seq=A;Dbxref=dbSNP_129:rs18963923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317769	317769	.	+	.	ID=4183;Variant_seq=T;Dbxref=dbSNP_129:rs18963933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317772	317772	.	+	.	ID=4184;Variant_seq=A;Dbxref=dbSNP_129:rs18963943;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317776	317776	.	+	.	ID=4185;Variant_seq=C;Dbxref=dbSNP_129:rs18963953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317777	317777	.	+	.	ID=4186;Variant_seq=A;Dbxref=dbSNP_129:rs18963963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317781	317781	.	+	.	ID=4187;Variant_seq=T;Dbxref=dbSNP_129:rs18963982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317788	317788	.	+	.	ID=4188;Variant_seq=C;Dbxref=dbSNP_129:rs18964002;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317793	317793	.	+	.	ID=4189;Variant_seq=C;Dbxref=dbSNP_129:rs18964032;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317794	317794	.	+	.	ID=4190;Variant_seq=A;Dbxref=dbSNP_129:rs18964042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317799	317799	.	+	.	ID=4191;Variant_seq=G;Dbxref=dbSNP_129:rs18964052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317800	317800	.	+	.	ID=4192;Variant_seq=G;Dbxref=dbSNP_129:rs18964062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317804	317804	.	+	.	ID=4193;Variant_seq=G;Dbxref=dbSNP_129:rs18964081;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317805	317805	.	+	.	ID=4194;Variant_seq=C;Dbxref=dbSNP_129:rs18964091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317807	317807	.	+	.	ID=4195;Variant_seq=T;Dbxref=dbSNP_129:rs18964101;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317808	317808	.	+	.	ID=4196;Variant_seq=T;Dbxref=dbSNP_129:rs18964111;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317809	317809	.	+	.	ID=4197;Variant_seq=T;Dbxref=dbSNP_129:rs18964121;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317812	317812	.	+	.	ID=4198;Variant_seq=G;Dbxref=dbSNP_129:rs18964141;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317817	317817	.	+	.	ID=4199;Variant_seq=A;Dbxref=dbSNP_129:rs18964161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317818	317818	.	+	.	ID=4200;Variant_seq=A;Dbxref=dbSNP_129:rs18964171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317819	317819	.	+	.	ID=4201;Variant_seq=G;Dbxref=dbSNP_129:rs18964181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317822	317822	.	+	.	ID=4202;Variant_seq=G;Dbxref=dbSNP_129:rs18964191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	317829	317829	.	+	.	ID=4203;Variant_seq=T;Dbxref=dbSNP_129:rs18964201;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317830	317830	.	+	.	ID=4204;Variant_seq=C;Dbxref=dbSNP_129:rs18964211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317832	317832	.	+	.	ID=4205;Variant_seq=A;Dbxref=dbSNP_129:rs18964221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317836	317836	.	+	.	ID=4206;Variant_seq=A;Dbxref=dbSNP_129:rs18964231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317840	317840	.	+	.	ID=4207;Variant_seq=C;Dbxref=dbSNP_129:rs18964251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317844	317844	.	+	.	ID=4208;Variant_seq=G;Dbxref=dbSNP_129:rs18964261;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317855	317855	.	+	.	ID=4209;Variant_seq=C;Dbxref=dbSNP_129:rs18964271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317860	317860	.	+	.	ID=4210;Variant_seq=C;Dbxref=dbSNP_129:rs18964281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	317865	317865	.	+	.	ID=4211;Variant_seq=T;Dbxref=dbSNP_129:rs18964301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	317866	317866	.	+	.	ID=4212;Variant_seq=C;Dbxref=dbSNP_129:rs18964311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	317867	317867	.	+	.	ID=4213;Variant_seq=C;Dbxref=dbSNP_129:rs18964321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318032	318032	.	+	.	ID=4214;Variant_seq=G;Dbxref=dbSNP_129:rs18964861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318035	318035	.	+	.	ID=4215;Variant_seq=C;Dbxref=dbSNP_129:rs18964871;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318037	318037	.	+	.	ID=4216;Variant_seq=C;Dbxref=dbSNP_129:rs18964881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318038	318038	.	+	.	ID=4217;Variant_seq=T;Dbxref=dbSNP_129:rs18964891;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318039	318039	.	+	.	ID=4218;Variant_seq=A;Dbxref=dbSNP_129:rs18964901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318041	318041	.	+	.	ID=4219;Variant_seq=G;Dbxref=dbSNP_129:rs18964911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318044	318044	.	+	.	ID=4220;Variant_seq=C;Dbxref=dbSNP_129:rs18964921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318118	318118	.	+	.	ID=4221;Variant_seq=T;Dbxref=dbSNP_129:rs18965151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318119	318119	.	+	.	ID=4222;Variant_seq=C;Dbxref=dbSNP_129:rs18965161;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318120	318120	.	+	.	ID=4223;Variant_seq=T;Dbxref=dbSNP_129:rs18965171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318121	318121	.	+	.	ID=4224;Variant_seq=C;Dbxref=dbSNP_129:rs18965181;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318125	318125	.	+	.	ID=4225;Variant_seq=C;Dbxref=dbSNP_129:rs18965191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318131	318131	.	+	.	ID=4226;Variant_seq=G;Dbxref=dbSNP_129:rs18965211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318137	318137	.	+	.	ID=4227;Variant_seq=C;Dbxref=dbSNP_129:rs18965221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318138	318138	.	+	.	ID=4228;Variant_seq=G;Dbxref=dbSNP_129:rs18965231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318143	318143	.	+	.	ID=4229;Variant_seq=T;Dbxref=dbSNP_129:rs18965241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318149	318149	.	+	.	ID=4230;Variant_seq=C;Dbxref=dbSNP_129:rs18965251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318154	318154	.	+	.	ID=4231;Variant_seq=C;Dbxref=dbSNP_129:rs18965291;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318157	318157	.	+	.	ID=4232;Variant_seq=T;Dbxref=dbSNP_129:rs18965301;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318158	318158	.	+	.	ID=4233;Variant_seq=G;Dbxref=dbSNP_129:rs18965311;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318159	318159	.	+	.	ID=4234;Variant_seq=C;Dbxref=dbSNP_129:rs18965321;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318161	318161	.	+	.	ID=4235;Variant_seq=G;Dbxref=dbSNP_129:rs18965331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318166	318166	.	+	.	ID=4236;Variant_seq=A;Dbxref=dbSNP_129:rs18965351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318169	318169	.	+	.	ID=4237;Variant_seq=A;Dbxref=dbSNP_129:rs18965361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318170	318170	.	+	.	ID=4238;Variant_seq=A;Dbxref=dbSNP_129:rs18965371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318173	318173	.	+	.	ID=4239;Variant_seq=T;Dbxref=dbSNP_129:rs18965381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318177	318177	.	+	.	ID=4240;Variant_seq=T;Dbxref=dbSNP_129:rs18965391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318180	318180	.	+	.	ID=4241;Variant_seq=A;Dbxref=dbSNP_129:rs18965401;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318181	318181	.	+	.	ID=4242;Variant_seq=T;Dbxref=dbSNP_129:rs18965411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318182	318182	.	+	.	ID=4243;Variant_seq=T;Dbxref=dbSNP_129:rs18965421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318265	318265	.	+	.	ID=4244;Variant_seq=G;Dbxref=dbSNP_129:rs18965761;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318266	318266	.	+	.	ID=4245;Variant_seq=G;Dbxref=dbSNP_129:rs18965771;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318273	318273	.	+	.	ID=4246;Variant_seq=T;Dbxref=dbSNP_129:rs18965781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318275	318275	.	+	.	ID=4247;Variant_seq=G;Dbxref=dbSNP_129:rs18965791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318278	318278	.	+	.	ID=4248;Variant_seq=T;Dbxref=dbSNP_129:rs18965811;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318280	318280	.	+	.	ID=4249;Variant_seq=C;Dbxref=dbSNP_129:rs18965821;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318287	318287	.	+	.	ID=4250;Variant_seq=A;Dbxref=dbSNP_129:rs18965840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318293	318293	.	+	.	ID=4251;Variant_seq=A;Dbxref=dbSNP_129:rs18965850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318296	318296	.	+	.	ID=4252;Variant_seq=C;Dbxref=dbSNP_129:rs18965860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318320	318320	.	+	.	ID=4253;Variant_seq=A;Dbxref=dbSNP_129:rs18965880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318322	318322	.	+	.	ID=4254;Variant_seq=T;Dbxref=dbSNP_129:rs18965890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318323	318323	.	+	.	ID=4255;Variant_seq=T;Dbxref=dbSNP_129:rs18965900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318326	318326	.	+	.	ID=4256;Variant_seq=T;Dbxref=dbSNP_129:rs18965910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318329	318329	.	+	.	ID=4257;Variant_seq=T;Dbxref=dbSNP_129:rs18965920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318333	318333	.	+	.	ID=4258;Variant_seq=T;Dbxref=dbSNP_129:rs18965950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318334	318334	.	+	.	ID=4259;Variant_seq=A;Dbxref=dbSNP_129:rs18965960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318335	318335	.	+	.	ID=4260;Variant_seq=A;Dbxref=dbSNP_129:rs18965970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318650	318650	.	+	.	ID=4261;Variant_seq=T;Dbxref=dbSNP_129:rs18967019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318725	318725	.	+	.	ID=4262;Variant_seq=C;Dbxref=dbSNP_129:rs18966140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318728	318728	.	+	.	ID=4263;Variant_seq=C;Dbxref=dbSNP_129:rs18966160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318729	318729	.	+	.	ID=4264;Variant_seq=C;Dbxref=dbSNP_129:rs18966170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318732	318732	.	+	.	ID=4265;Variant_seq=C;Dbxref=dbSNP_129:rs18966190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318734	318734	.	+	.	ID=4266;Variant_seq=A;Dbxref=dbSNP_129:rs18966200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318735	318735	.	+	.	ID=4267;Variant_seq=A;Dbxref=dbSNP_129:rs18966210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318736	318736	.	+	.	ID=4268;Variant_seq=T;Dbxref=dbSNP_129:rs18966220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318738	318738	.	+	.	ID=4269;Variant_seq=G;Dbxref=dbSNP_129:rs18966230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318740	318740	.	+	.	ID=4270;Variant_seq=T;Dbxref=dbSNP_129:rs18966250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318741	318741	.	+	.	ID=4271;Variant_seq=T;Dbxref=dbSNP_129:rs18966260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318744	318744	.	+	.	ID=4272;Variant_seq=T;Dbxref=dbSNP_129:rs18966290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318745	318745	.	+	.	ID=4273;Variant_seq=C;Dbxref=dbSNP_129:rs18966300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318746	318746	.	+	.	ID=4274;Variant_seq=T;Dbxref=dbSNP_129:rs18966310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	318748	318748	.	+	.	ID=4275;Variant_seq=T;Dbxref=dbSNP_129:rs18966320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318758	318758	.	+	.	ID=4276;Variant_seq=C;Dbxref=dbSNP_129:rs18966340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318759	318759	.	+	.	ID=4277;Variant_seq=A;Dbxref=dbSNP_129:rs18966350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318764	318764	.	+	.	ID=4278;Variant_seq=G;Dbxref=dbSNP_129:rs18966370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318766	318766	.	+	.	ID=4279;Variant_seq=T;Dbxref=dbSNP_129:rs18966380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	318884	318884	.	+	.	ID=4280;Variant_seq=A;Dbxref=dbSNP_129:rs18966709;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	318885	318885	.	+	.	ID=4281;Variant_seq=A;Dbxref=dbSNP_129:rs18966719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318886	318886	.	+	.	ID=4282;Variant_seq=A;Dbxref=dbSNP_129:rs18966729;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	318889	318889	.	+	.	ID=4283;Variant_seq=A;Dbxref=dbSNP_129:rs18966739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	361110	361110	.	+	.	ID=4284;Variant_seq=A;Dbxref=dbSNP_129:rs53658684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	361111	361111	.	+	.	ID=4285;Variant_seq=A;Dbxref=dbSNP_129:rs52957632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	363415	363415	.	+	.	ID=4286;Variant_seq=T;Dbxref=dbSNP_129:rs18970810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	363487	363487	.	+	.	ID=4287;Variant_seq=T;Dbxref=dbSNP_129:rs18970820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	377845	377845	.	+	.	ID=4288;Variant_seq=A;Dbxref=dbSNP_129:rs53658684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	377846	377846	.	+	.	ID=4289;Variant_seq=A;Dbxref=dbSNP_129:rs52957632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	386775	386775	.	+	.	ID=4290;Variant_seq=A;Dbxref=dbSNP_129:rs18970440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	399009	399009	.	+	.	ID=4291;Variant_seq=C;Dbxref=dbSNP_129:rs18970810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	399081	399081	.	+	.	ID=4292;Variant_seq=C;Dbxref=dbSNP_129:rs18970820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	412090	412090	.	+	.	ID=4293;Variant_seq=C;Dbxref=dbSNP_129:rs21344503;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	420221	420221	.	+	.	ID=4294;Variant_seq=C;Dbxref=dbSNP_129:rs18971990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	420685	420685	.	+	.	ID=4295;Variant_seq=C;Dbxref=dbSNP_129:rs17898505;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	422939	422939	.	+	.	ID=4296;Variant_seq=C;Dbxref=dbSNP_129:rs53336547;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	446871	446871	.	+	.	ID=4297;Variant_seq=T;Dbxref=dbSNP_129:rs18971990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	447962	447962	.	+	.	ID=4298;Variant_seq=G;Dbxref=dbSNP_129:rs18970440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	448725	448725	.	+	.	ID=4299;Variant_seq=G;Dbxref=dbSNP_129:rs20391595;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	454882	454882	.	+	.	ID=4300;Variant_seq=T;Dbxref=dbSNP_129:rs18973827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	465464	465464	.	+	.	ID=4301;Variant_seq=T;Dbxref=dbSNP_129:rs18974336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	468948	468948	.	+	.	ID=4302;Variant_seq=T;Dbxref=dbSNP_129:rs18974435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	469113	469113	.	+	.	ID=4303;Variant_seq=G;Dbxref=dbSNP_129:rs18974467;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	469863	469863	.	+	.	ID=4304;Variant_seq=T;Dbxref=dbSNP_129:rs18974680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	471188	471188	.	+	.	ID=4305;Variant_seq=C;Dbxref=dbSNP_129:rs18974730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	471244	471244	.	+	.	ID=4306;Variant_seq=A;Dbxref=dbSNP_129:rs18974740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	479868	479868	.	+	.	ID=4307;Variant_seq=A;Dbxref=dbSNP_129:rs53465413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	479892	479892	.	+	.	ID=4308;Variant_seq=G;Dbxref=dbSNP_129:rs54337135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	479893	479893	.	+	.	ID=4309;Variant_seq=T;Dbxref=dbSNP_129:rs53062390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	479906	479906	.	+	.	ID=4310;Variant_seq=T;Dbxref=dbSNP_129:rs53503632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	479907	479907	.	+	.	ID=4311;Variant_seq=T;Dbxref=dbSNP_129:rs53553312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	479917	479917	.	+	.	ID=4312;Variant_seq=A;Dbxref=dbSNP_129:rs52939281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	479945	479945	.	+	.	ID=4313;Variant_seq=C;Dbxref=dbSNP_129:rs53703711;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	480039	480039	.	+	.	ID=4314;Variant_seq=G;Dbxref=dbSNP_129:rs53550870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	480066	480066	.	+	.	ID=4315;Variant_seq=G;Dbxref=dbSNP_129:rs54134031;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	480067	480067	.	+	.	ID=4316;Variant_seq=T;Dbxref=dbSNP_129:rs53813502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	480072	480072	.	+	.	ID=4317;Variant_seq=C;Dbxref=dbSNP_129:rs54299559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	480081	480081	.	+	.	ID=4318;Variant_seq=C;Dbxref=dbSNP_129:rs54018558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	480086	480086	.	+	.	ID=4319;Variant_seq=G;Dbxref=dbSNP_129:rs54102280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	480111	480111	.	+	.	ID=4320;Variant_seq=AGAAATGAAATTGTTCC;Dbxref=dbSNP_129:rs54294264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	480122	480122	.	+	.	ID=4321;Variant_seq=A;Dbxref=dbSNP_129:rs54343352;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	480143	480143	.	+	.	ID=4322;Variant_seq=T;Dbxref=dbSNP_129:rs53189799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	480148	480148	.	+	.	ID=4323;Variant_seq=C;Dbxref=dbSNP_129:rs54125237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	480165	480165	.	+	.	ID=4324;Variant_seq=C;Dbxref=dbSNP_129:rs53339718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	480907	480907	.	+	.	ID=4325;Variant_seq=T;Dbxref=dbSNP_129:rs18976214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	481318	481318	.	+	.	ID=4326;Variant_seq=T;Dbxref=dbSNP_129:rs18976244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	481750	481750	.	+	.	ID=4327;Variant_seq=G;Dbxref=dbSNP_129:rs18976344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	494459	494459	.	+	.	ID=4328;Variant_seq=A;Dbxref=dbSNP_129:rs53882981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	494501	494501	.	+	.	ID=4329;Variant_seq=A;Dbxref=dbSNP_129:rs21333660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	495788	495788	.	+	.	ID=4330;Variant_seq=G;Dbxref=dbSNP_129:rs18978382;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496013	496013	.	+	.	ID=4331;Variant_seq=T;Dbxref=dbSNP_129:rs20672152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496023	496023	.	+	.	ID=4332;Variant_seq=A;Dbxref=dbSNP_129:rs18978412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496037	496037	.	+	.	ID=4333;Variant_seq=G;Dbxref=dbSNP_129:rs20672132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496047	496047	.	+	.	ID=4334;Variant_seq=T;Dbxref=dbSNP_129:rs18978452;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496061	496061	.	+	.	ID=4335;Variant_seq=A,C;Dbxref=dbSNP_129:rs17895062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496073	496073	.	+	.	ID=4336;Variant_seq=A;Dbxref=dbSNP_129:rs20672062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496107	496107	.	+	.	ID=4337;Variant_seq=G;Dbxref=dbSNP_129:rs18978502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496322	496322	.	+	.	ID=4338;Variant_seq=G;Dbxref=dbSNP_129:rs18978562;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496328	496328	.	+	.	ID=4339;Variant_seq=A;Dbxref=dbSNP_129:rs18978582;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496331	496331	.	+	.	ID=4340;Variant_seq=G;Dbxref=dbSNP_129:rs18978592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496340	496340	.	+	.	ID=4341;Variant_seq=G;Dbxref=dbSNP_129:rs18978612;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496342	496342	.	+	.	ID=4342;Variant_seq=G;Dbxref=dbSNP_129:rs18978622;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496349	496349	.	+	.	ID=4343;Variant_seq=G;Dbxref=dbSNP_129:rs17892179;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496361	496361	.	+	.	ID=4344;Variant_seq=C;Dbxref=dbSNP_129:rs18978632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496376	496376	.	+	.	ID=4345;Variant_seq=C;Dbxref=dbSNP_129:rs18978642;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496492	496492	.	+	.	ID=4346;Variant_seq=G;Dbxref=dbSNP_129:rs18978702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496526	496526	.	+	.	ID=4347;Variant_seq=C;Dbxref=dbSNP_129:rs18978712;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496529	496529	.	+	.	ID=4348;Variant_seq=T;Dbxref=dbSNP_129:rs18978732;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496532	496532	.	+	.	ID=4349;Variant_seq=C;Dbxref=dbSNP_129:rs18978742;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496545	496545	.	+	.	ID=4350;Variant_seq=T;Dbxref=dbSNP_129:rs18978752;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	496549	496549	.	+	.	ID=4351;Variant_seq=A,C,G;Dbxref=dbSNP_129:rs17893762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496552	496552	.	+	.	ID=4352;Variant_seq=T;Dbxref=dbSNP_129:rs18978762;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496553	496553	.	+	.	ID=4353;Variant_seq=G;Dbxref=dbSNP_129:rs18978772;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496557	496557	.	+	.	ID=4354;Variant_seq=A;Dbxref=dbSNP_129:rs18978782;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496559	496559	.	+	.	ID=4355;Variant_seq=A;Dbxref=dbSNP_129:rs18978792;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496561	496561	.	+	.	ID=4356;Variant_seq=T;Dbxref=dbSNP_129:rs18978802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	496568	496568	.	+	.	ID=4357;Variant_seq=T;Dbxref=dbSNP_129:rs18978832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496569	496569	.	+	.	ID=4358;Variant_seq=A;Dbxref=dbSNP_129:rs18978842;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496571	496571	.	+	.	ID=4359;Variant_seq=T;Dbxref=dbSNP_129:rs18978852;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496573	496573	.	+	.	ID=4360;Variant_seq=T;Dbxref=dbSNP_129:rs18978862;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496593	496593	.	+	.	ID=4361;Variant_seq=A;Dbxref=dbSNP_129:rs18978892;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496598	496598	.	+	.	ID=4362;Variant_seq=G;Dbxref=dbSNP_129:rs18978902;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496601	496601	.	+	.	ID=4363;Variant_seq=C;Dbxref=dbSNP_129:rs18978912;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496605	496605	.	+	.	ID=4364;Variant_seq=A;Dbxref=dbSNP_129:rs18978922;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496608	496608	.	+	.	ID=4365;Variant_seq=G;Dbxref=dbSNP_129:rs18978932;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496610	496610	.	+	.	ID=4366;Variant_seq=C;Dbxref=dbSNP_129:rs18978942;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496630	496630	.	+	.	ID=4367;Variant_seq=T;Dbxref=dbSNP_129:rs18978992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	496633	496633	.	+	.	ID=4368;Variant_seq=T;Dbxref=dbSNP_129:rs18979002;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496657	496657	.	+	.	ID=4369;Variant_seq=C;Dbxref=dbSNP_129:rs18979052;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496671	496671	.	+	.	ID=4370;Variant_seq=A;Dbxref=dbSNP_129:rs18979092;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496702	496702	.	+	.	ID=4371;Variant_seq=C;Dbxref=dbSNP_129:rs18979142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496711	496711	.	+	.	ID=4372;Variant_seq=T;Dbxref=dbSNP_129:rs18979152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	496714	496714	.	+	.	ID=4373;Variant_seq=C;Dbxref=dbSNP_129:rs18979162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496716	496716	.	+	.	ID=4374;Variant_seq=C;Dbxref=dbSNP_129:rs18979172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	496721	496721	.	+	.	ID=4375;Variant_seq=C;Dbxref=dbSNP_129:rs18979192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	496742	496742	.	+	.	ID=4376;Variant_seq=T;Dbxref=dbSNP_129:rs18979212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	496766	496766	.	+	.	ID=4377;Variant_seq=G;Dbxref=dbSNP_129:rs18979232;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	497448	497448	.	+	.	ID=4378;Variant_seq=C;Dbxref=dbSNP_129:rs52902129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	497517	497517	.	+	.	ID=4379;Variant_seq=A;Dbxref=dbSNP_129:rs54104319;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	497524	497524	.	+	.	ID=4380;Variant_seq=T;Dbxref=dbSNP_129:rs53295877;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	497630	497630	.	+	.	ID=4381;Variant_seq=CTCCTCGACCGAGGGTCTTTTTCACCACCATGGGTCTT;Dbxref=dbSNP_129:rs53784916;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	502837	502837	.	+	.	ID=4382;Variant_seq=C;Dbxref=dbSNP_129:rs18974336;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	504964	504964	.	+	.	ID=4383;Variant_seq=C;Dbxref=dbSNP_129:rs18974435;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	505129	505129	.	+	.	ID=4384;Variant_seq=A;Dbxref=dbSNP_129:rs18974467;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	505880	505880	.	+	.	ID=4385;Variant_seq=C;Dbxref=dbSNP_129:rs18974680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	506292	506292	.	+	.	ID=4386;Variant_seq=A;Dbxref=dbSNP_129:rs53465413;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	506316	506316	.	+	.	ID=4387;Variant_seq=G;Dbxref=dbSNP_129:rs54337135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	506317	506317	.	+	.	ID=4388;Variant_seq=T;Dbxref=dbSNP_129:rs53062390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	506330	506330	.	+	.	ID=4389;Variant_seq=T;Dbxref=dbSNP_129:rs53503632;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	506331	506331	.	+	.	ID=4390;Variant_seq=T;Dbxref=dbSNP_129:rs53553312;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	506341	506341	.	+	.	ID=4391;Variant_seq=A;Dbxref=dbSNP_129:rs52939281;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	506369	506369	.	+	.	ID=4392;Variant_seq=C;Dbxref=dbSNP_129:rs53703711;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	506463	506463	.	+	.	ID=4393;Variant_seq=G;Dbxref=dbSNP_129:rs53550870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	506490	506490	.	+	.	ID=4394;Variant_seq=G;Dbxref=dbSNP_129:rs54134031;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	506491	506491	.	+	.	ID=4395;Variant_seq=T;Dbxref=dbSNP_129:rs53813502;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	506496	506496	.	+	.	ID=4396;Variant_seq=C;Dbxref=dbSNP_129:rs54299559;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	506505	506505	.	+	.	ID=4397;Variant_seq=C;Dbxref=dbSNP_129:rs54018558;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	506510	506510	.	+	.	ID=4398;Variant_seq=G;Dbxref=dbSNP_129:rs54102280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	506535	506535	.	+	.	ID=4399;Variant_seq=AGAAATGAAATTGTTCC;Dbxref=dbSNP_129:rs54294264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	506546	506546	.	+	.	ID=4400;Variant_seq=A;Dbxref=dbSNP_129:rs54343352;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	506567	506567	.	+	.	ID=4401;Variant_seq=T;Dbxref=dbSNP_129:rs53189799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	506572	506572	.	+	.	ID=4402;Variant_seq=C;Dbxref=dbSNP_129:rs54125237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	506589	506589	.	+	.	ID=4403;Variant_seq=C;Dbxref=dbSNP_129:rs53339718;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	507309	507309	.	+	.	ID=4404;Variant_seq=C;Dbxref=dbSNP_129:rs18976214;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	507719	507719	.	+	.	ID=4405;Variant_seq=G;Dbxref=dbSNP_129:rs18976244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	508156	508156	.	+	.	ID=4406;Variant_seq=A;Dbxref=dbSNP_129:rs18976344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	511561	511561	.	+	.	ID=4407;Variant_seq=C;Dbxref=dbSNP_129:rs54129481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	531448	531448	.	+	.	ID=4408;Variant_seq=T;Dbxref=dbSNP_129:rs19638992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	534156	534156	.	+	.	ID=4409;Variant_seq=C;Dbxref=dbSNP_129:rs17929861;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	534160	534160	.	+	.	ID=4410;Variant_seq=G;Dbxref=dbSNP_129:rs17929879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534171	534171	.	+	.	ID=4411;Variant_seq=T;Dbxref=dbSNP_129:rs20759602;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534560	534560	.	+	.	ID=4412;Variant_seq=C;Dbxref=dbSNP_129:rs20986036;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534563	534563	.	+	.	ID=4413;Variant_seq=A;Dbxref=dbSNP_129:rs20986026;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	534565	534565	.	+	.	ID=4414;Variant_seq=A;Dbxref=dbSNP_129:rs20986016;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	534568	534568	.	+	.	ID=4415;Variant_seq=G;Dbxref=dbSNP_129:rs20986006;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534569	534569	.	+	.	ID=4416;Variant_seq=T;Dbxref=dbSNP_129:rs20985996;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	534577	534577	.	+	.	ID=4417;Variant_seq=G;Dbxref=dbSNP_129:rs20985976;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534584	534584	.	+	.	ID=4418;Variant_seq=G;Dbxref=dbSNP_129:rs20985956;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534587	534587	.	+	.	ID=4419;Variant_seq=T;Dbxref=dbSNP_129:rs20985946;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	534596	534596	.	+	.	ID=4420;Variant_seq=G;Dbxref=dbSNP_129:rs20985936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	534600	534600	.	+	.	ID=4421;Variant_seq=C;Dbxref=dbSNP_129:rs20985926;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	538414	538414	.	+	.	ID=4422;Variant_seq=A;Dbxref=dbSNP_129:rs18980461;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	538515	538515	.	+	.	ID=4423;Variant_seq=C;Dbxref=dbSNP_129:rs18980471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	538919	538919	.	+	.	ID=4424;Variant_seq=A;Dbxref=dbSNP_129:rs18980481;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	538930	538930	.	+	.	ID=4425;Variant_seq=T;Dbxref=dbSNP_129:rs18980491;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	542796	542796	.	+	.	ID=4426;Variant_seq=T;Dbxref=dbSNP_129:rs18980871;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	542806	542806	.	+	.	ID=4427;Variant_seq=C;Dbxref=dbSNP_129:rs18144739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	542807	542807	.	+	.	ID=4428;Variant_seq=C;Dbxref=dbSNP_129:rs18144748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	545972	545972	.	+	.	ID=4429;Variant_seq=A;Dbxref=dbSNP_129:rs18974730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	546028	546028	.	+	.	ID=4430;Variant_seq=T;Dbxref=dbSNP_129:rs18974740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	558700	558700	.	+	.	ID=4431;Variant_seq=C;Dbxref=dbSNP_129:rs18981812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	558773	558773	.	+	.	ID=4432;Variant_seq=C;Dbxref=dbSNP_129:rs18981822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	558782	558782	.	+	.	ID=4433;Variant_seq=C;Dbxref=dbSNP_129:rs18981832;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	581360	581360	.	+	.	ID=4434;Variant_seq=A;Dbxref=dbSNP_129:rs54291371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	608706	608706	.	+	.	ID=4435;Variant_seq=TCATGT;Dbxref=dbSNP_129:rs53540278;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	insertion	608708	608708	.	+	.	ID=4436;Variant_seq=T;Dbxref=dbSNP_129:rs53155322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	608720	608720	.	+	.	ID=4437;Variant_seq=T;Dbxref=dbSNP_129:rs53121490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	608802	608802	.	+	.	ID=4438;Variant_seq=A;Dbxref=dbSNP_129:rs53246114;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	608818	608818	.	+	.	ID=4439;Variant_seq=T;Dbxref=dbSNP_129:rs53136096;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	608823	608823	.	+	.	ID=4440;Variant_seq=T;Dbxref=dbSNP_129:rs52875810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	608826	608826	.	+	.	ID=4441;Variant_seq=C;Dbxref=dbSNP_129:rs54252131;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	608839	608840	.	+	.	ID=4442;Variant_seq=-;Dbxref=dbSNP_129:rs54069118;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TA
5	dbSNP	SNV	608862	608862	.	+	.	ID=4443;Variant_seq=A;Dbxref=dbSNP_129:rs53669941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	608874	608874	.	+	.	ID=4444;Variant_seq=CACAACTAATAA;Dbxref=dbSNP_129:rs53525753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	608880	608880	.	+	.	ID=4445;Variant_seq=C;Dbxref=dbSNP_129:rs54285377;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	608905	608905	.	+	.	ID=4446;Variant_seq=C;Dbxref=dbSNP_129:rs54278142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	609746	609746	.	+	.	ID=4447;Variant_seq=A;Dbxref=dbSNP_129:rs18985003;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	622464	622464	.	+	.	ID=4448;Variant_seq=A;Dbxref=dbSNP_129:rs19942114;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	622465	622465	.	+	.	ID=4449;Variant_seq=A;Dbxref=dbSNP_129:rs19942124;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	622466	622466	.	+	.	ID=4450;Variant_seq=A;Dbxref=dbSNP_129:rs19942134;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	622469	622469	.	+	.	ID=4451;Variant_seq=C;Dbxref=dbSNP_129:rs19942144;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	622472	622472	.	+	.	ID=4452;Variant_seq=T;Dbxref=dbSNP_129:rs19942154;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	622477	622477	.	+	.	ID=4453;Variant_seq=T;Dbxref=dbSNP_129:rs19942164;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	622483	622483	.	+	.	ID=4454;Variant_seq=T;Dbxref=dbSNP_129:rs19942174;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	622488	622488	.	+	.	ID=4455;Variant_seq=T;Dbxref=dbSNP_129:rs19942184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	622641	622641	.	+	.	ID=4456;Variant_seq=G;Dbxref=dbSNP_129:rs18984973;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	622863	622863	.	+	.	ID=4457;Variant_seq=C;Dbxref=dbSNP_129:rs18984983;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	622872	622872	.	+	.	ID=4458;Variant_seq=A;Dbxref=dbSNP_129:rs18984993;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	625335	625335	.	+	.	ID=4459;Variant_seq=TCATGT;Dbxref=dbSNP_129:rs53540278;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	insertion	625337	625337	.	+	.	ID=4460;Variant_seq=T;Dbxref=dbSNP_129:rs53155322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	625349	625349	.	+	.	ID=4461;Variant_seq=T;Dbxref=dbSNP_129:rs53121490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	625431	625431	.	+	.	ID=4462;Variant_seq=A;Dbxref=dbSNP_129:rs53246114;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	625447	625447	.	+	.	ID=4463;Variant_seq=T;Dbxref=dbSNP_129:rs53136096;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	625452	625452	.	+	.	ID=4464;Variant_seq=T;Dbxref=dbSNP_129:rs52875810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	625455	625455	.	+	.	ID=4465;Variant_seq=C;Dbxref=dbSNP_129:rs54252131;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	625468	625469	.	+	.	ID=4466;Variant_seq=-;Dbxref=dbSNP_129:rs54069118;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TA
5	dbSNP	SNV	625491	625491	.	+	.	ID=4467;Variant_seq=A;Dbxref=dbSNP_129:rs53669941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	insertion	625503	625503	.	+	.	ID=4468;Variant_seq=CACAACTAATAA;Dbxref=dbSNP_129:rs53525753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	625509	625509	.	+	.	ID=4469;Variant_seq=C;Dbxref=dbSNP_129:rs54285377;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	625534	625534	.	+	.	ID=4470;Variant_seq=C;Dbxref=dbSNP_129:rs54278142;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	626373	626373	.	+	.	ID=4471;Variant_seq=G;Dbxref=dbSNP_129:rs18985003;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	627253	627253	.	+	.	ID=4472;Variant_seq=T;Dbxref=dbSNP_129:rs53629897;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	627256	627256	.	+	.	ID=4473;Variant_seq=A;Dbxref=dbSNP_129:rs53952684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	627268	627268	.	+	.	ID=4474;Variant_seq=C;Dbxref=dbSNP_129:rs53013593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	627281	627281	.	+	.	ID=4475;Variant_seq=A;Dbxref=dbSNP_129:rs53284191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	627301	627301	.	+	.	ID=4476;Variant_seq=G;Dbxref=dbSNP_129:rs53676938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	627302	627302	.	+	.	ID=4477;Variant_seq=A;Dbxref=dbSNP_129:rs53461288;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	627309	627309	.	+	.	ID=4478;Variant_seq=A;Dbxref=dbSNP_129:rs52997585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	627322	627322	.	+	.	ID=4479;Variant_seq=C;Dbxref=dbSNP_129:rs53563471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	627341	627341	.	+	.	ID=4480;Variant_seq=A;Dbxref=dbSNP_129:rs53532122;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	627346	627346	.	+	.	ID=4481;Variant_seq=G;Dbxref=dbSNP_129:rs53720646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	627457	627457	.	+	.	ID=4482;Variant_seq=A;Dbxref=dbSNP_129:rs54080773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	628091	628091	.	+	.	ID=4483;Variant_seq=G;Dbxref=dbSNP_129:rs54314400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	628093	628093	.	+	.	ID=4484;Variant_seq=T;Dbxref=dbSNP_129:rs52845815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	628096	628096	.	+	.	ID=4485;Variant_seq=T;Dbxref=dbSNP_129:rs53952200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	628585	628585	.	+	.	ID=4486;Variant_seq=A;Dbxref=dbSNP_129:rs54055882;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	628590	628590	.	+	.	ID=4487;Variant_seq=A;Dbxref=dbSNP_129:rs53025694;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	628595	628595	.	+	.	ID=4488;Variant_seq=T;Dbxref=dbSNP_129:rs54373529;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	628596	628596	.	+	.	ID=4489;Variant_seq=A;Dbxref=dbSNP_129:rs53722853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	628604	628604	.	+	.	ID=4490;Variant_seq=A;Dbxref=dbSNP_129:rs53257344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	628608	628608	.	+	.	ID=4491;Variant_seq=A;Dbxref=dbSNP_129:rs53017948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	628612	628612	.	+	.	ID=4492;Variant_seq=C;Dbxref=dbSNP_129:rs53064541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	636152	636152	.	+	.	ID=4493;Variant_seq=T;Dbxref=dbSNP_129:rs53629897;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	636155	636155	.	+	.	ID=4494;Variant_seq=A;Dbxref=dbSNP_129:rs53952684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	636167	636167	.	+	.	ID=4495;Variant_seq=C;Dbxref=dbSNP_129:rs53013593;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	636180	636180	.	+	.	ID=4496;Variant_seq=A;Dbxref=dbSNP_129:rs53284191;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	636200	636200	.	+	.	ID=4497;Variant_seq=G;Dbxref=dbSNP_129:rs53676938;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	636201	636201	.	+	.	ID=4498;Variant_seq=A;Dbxref=dbSNP_129:rs53461288;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	636208	636208	.	+	.	ID=4499;Variant_seq=A;Dbxref=dbSNP_129:rs52997585;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	636221	636221	.	+	.	ID=4500;Variant_seq=C;Dbxref=dbSNP_129:rs53563471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	636240	636240	.	+	.	ID=4501;Variant_seq=A;Dbxref=dbSNP_129:rs53532122;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	636245	636245	.	+	.	ID=4502;Variant_seq=G;Dbxref=dbSNP_129:rs53720646;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	636356	636356	.	+	.	ID=4503;Variant_seq=G;Dbxref=dbSNP_129:rs54080773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	636996	636996	.	+	.	ID=4504;Variant_seq=G;Dbxref=dbSNP_129:rs54314400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	636998	636998	.	+	.	ID=4505;Variant_seq=T;Dbxref=dbSNP_129:rs52845815;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	637001	637001	.	+	.	ID=4506;Variant_seq=T;Dbxref=dbSNP_129:rs53952200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	637467	637467	.	+	.	ID=4507;Variant_seq=A;Dbxref=dbSNP_129:rs54055882;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	637472	637472	.	+	.	ID=4508;Variant_seq=A;Dbxref=dbSNP_129:rs53025694;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	637477	637477	.	+	.	ID=4509;Variant_seq=T;Dbxref=dbSNP_129:rs54373529;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	637478	637478	.	+	.	ID=4510;Variant_seq=A;Dbxref=dbSNP_129:rs53722853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	637486	637486	.	+	.	ID=4511;Variant_seq=A;Dbxref=dbSNP_129:rs53257344;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	637490	637490	.	+	.	ID=4512;Variant_seq=A;Dbxref=dbSNP_129:rs53017948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	637494	637494	.	+	.	ID=4513;Variant_seq=C;Dbxref=dbSNP_129:rs53064541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	650685	650685	.	+	.	ID=4514;Variant_seq=T;Dbxref=dbSNP_129:rs18745245;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	652121	652121	.	+	.	ID=4515;Variant_seq=A;Dbxref=dbSNP_129:rs18279306;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	652126	652126	.	+	.	ID=4516;Variant_seq=T;Dbxref=dbSNP_129:rs18279324;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	652163	652163	.	+	.	ID=4517;Variant_seq=A;Dbxref=dbSNP_129:rs18279333;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	652270	652270	.	+	.	ID=4518;Variant_seq=T;Dbxref=dbSNP_129:rs18279360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	652364	652364	.	+	.	ID=4519;Variant_seq=T;Dbxref=dbSNP_129:rs18279369;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	652637	652637	.	+	.	ID=4520;Variant_seq=A;Dbxref=dbSNP_129:rs52842042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	652643	652643	.	+	.	ID=4521;Variant_seq=A;Dbxref=dbSNP_129:rs53689274;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	652694	652694	.	+	.	ID=4522;Variant_seq=G;Dbxref=dbSNP_129:rs18985802;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	652761	652761	.	+	.	ID=4523;Variant_seq=C;Dbxref=dbSNP_129:rs18985812;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	672065	672065	.	+	.	ID=4524;Variant_seq=C;Dbxref=dbSNP_129:rs52951969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	672091	672091	.	+	.	ID=4525;Variant_seq=T;Dbxref=dbSNP_129:rs53334877;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	672093	672093	.	+	.	ID=4526;Variant_seq=G;Dbxref=dbSNP_129:rs53145701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	deletion	672109	672114	.	+	.	ID=4527;Variant_seq=-;Dbxref=dbSNP_129:rs53890682;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AACTCC
5	dbSNP	SNV	672124	672124	.	+	.	ID=4528;Variant_seq=C;Dbxref=dbSNP_129:rs53888437;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	672756	672756	.	+	.	ID=4529;Variant_seq=A;Dbxref=dbSNP_129:rs18987612;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	672912	672912	.	+	.	ID=4530;Variant_seq=T;Dbxref=dbSNP_129:rs18987622;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	673301	673301	.	+	.	ID=4531;Variant_seq=A;Dbxref=dbSNP_129:rs18987652;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	673664	673664	.	+	.	ID=4532;Variant_seq=C;Dbxref=dbSNP_129:rs18986862;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	676376	676376	.	+	.	ID=4533;Variant_seq=G;Dbxref=dbSNP_129:rs18986912;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	676439	676439	.	+	.	ID=4534;Variant_seq=C;Dbxref=dbSNP_129:rs18986942;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	676454	676454	.	+	.	ID=4535;Variant_seq=C;Dbxref=dbSNP_129:rs18986952;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	676478	676478	.	+	.	ID=4536;Variant_seq=A;Dbxref=dbSNP_129:rs18986962;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	676584	676584	.	+	.	ID=4537;Variant_seq=A;Dbxref=dbSNP_129:rs18987022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	676748	676748	.	+	.	ID=4538;Variant_seq=C;Dbxref=dbSNP_129:rs18987092;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	676752	676752	.	+	.	ID=4539;Variant_seq=G;Dbxref=dbSNP_129:rs18987112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	676795	676795	.	+	.	ID=4540;Variant_seq=T;Dbxref=dbSNP_129:rs18987132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	683589	683589	.	+	.	ID=4541;Variant_seq=A;Dbxref=dbSNP_129:rs17969314;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	684132	684132	.	+	.	ID=4542;Variant_seq=T;Dbxref=dbSNP_129:rs18987402;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	684152	684152	.	+	.	ID=4543;Variant_seq=A;Dbxref=dbSNP_129:rs21150132;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	684172	684172	.	+	.	ID=4544;Variant_seq=T;Dbxref=dbSNP_129:rs18987412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	687074	687074	.	+	.	ID=4545;Variant_seq=C;Dbxref=dbSNP_129:rs52951969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	687100	687100	.	+	.	ID=4546;Variant_seq=T;Dbxref=dbSNP_129:rs53334877;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	687102	687102	.	+	.	ID=4547;Variant_seq=G;Dbxref=dbSNP_129:rs53145701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	deletion	687118	687123	.	+	.	ID=4548;Variant_seq=-;Dbxref=dbSNP_129:rs53890682;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AACTCC
5	dbSNP	SNV	687133	687133	.	+	.	ID=4549;Variant_seq=C;Dbxref=dbSNP_129:rs53888437;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	687765	687765	.	+	.	ID=4550;Variant_seq=G;Dbxref=dbSNP_129:rs18987612;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	687921	687921	.	+	.	ID=4551;Variant_seq=C;Dbxref=dbSNP_129:rs18987622;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	688310	688310	.	+	.	ID=4552;Variant_seq=G;Dbxref=dbSNP_129:rs18987652;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	688673	688673	.	+	.	ID=4553;Variant_seq=C;Dbxref=dbSNP_129:rs18986862;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	691888	691888	.	+	.	ID=4554;Variant_seq=A;Dbxref=dbSNP_129:rs52937468;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	696217	696217	.	+	.	ID=4555;Variant_seq=A;Dbxref=dbSNP_129:rs19836671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	697536	697536	.	+	.	ID=4556;Variant_seq=G;Dbxref=dbSNP_129:rs19836172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	698369	698369	.	+	.	ID=4557;Variant_seq=A;Dbxref=dbSNP_129:rs18036515;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	698376	698376	.	+	.	ID=4558;Variant_seq=A;Dbxref=dbSNP_129:rs18036506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	701590	701590	.	+	.	ID=4559;Variant_seq=A;Dbxref=dbSNP_129:rs19836671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	707490	707490	.	+	.	ID=4560;Variant_seq=G;Dbxref=dbSNP_129:rs18989341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	707495	707495	.	+	.	ID=4561;Variant_seq=C;Dbxref=dbSNP_129:rs18989371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	707497	707497	.	+	.	ID=4562;Variant_seq=T;Dbxref=dbSNP_129:rs18989381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	707501	707501	.	+	.	ID=4563;Variant_seq=A;Dbxref=dbSNP_129:rs18989391;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	707505	707505	.	+	.	ID=4564;Variant_seq=G;Dbxref=dbSNP_129:rs18989411;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	707511	707511	.	+	.	ID=4565;Variant_seq=G;Dbxref=dbSNP_129:rs18989421;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	707515	707515	.	+	.	ID=4566;Variant_seq=A;Dbxref=dbSNP_129:rs18989441;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709601	709601	.	+	.	ID=4567;Variant_seq=G;Dbxref=dbSNP_129:rs18995799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709604	709604	.	+	.	ID=4568;Variant_seq=A;Dbxref=dbSNP_129:rs18995819;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709605	709605	.	+	.	ID=4569;Variant_seq=G;Dbxref=dbSNP_129:rs18995829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709607	709607	.	+	.	ID=4570;Variant_seq=T;Dbxref=dbSNP_129:rs18995839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709609	709609	.	+	.	ID=4571;Variant_seq=G;Dbxref=dbSNP_129:rs18995849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709610	709610	.	+	.	ID=4572;Variant_seq=A;Dbxref=dbSNP_129:rs18995859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709611	709611	.	+	.	ID=4573;Variant_seq=T;Dbxref=dbSNP_129:rs18995869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709612	709612	.	+	.	ID=4574;Variant_seq=A;Dbxref=dbSNP_129:rs18995879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709616	709616	.	+	.	ID=4575;Variant_seq=G;Dbxref=dbSNP_129:rs18995889;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709623	709623	.	+	.	ID=4576;Variant_seq=C;Dbxref=dbSNP_129:rs18995899;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709624	709624	.	+	.	ID=4577;Variant_seq=G;Dbxref=dbSNP_129:rs18995909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709627	709627	.	+	.	ID=4578;Variant_seq=G;Dbxref=dbSNP_129:rs18995929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709632	709632	.	+	.	ID=4579;Variant_seq=G;Dbxref=dbSNP_129:rs18995939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709634	709634	.	+	.	ID=4580;Variant_seq=C;Dbxref=dbSNP_129:rs18995949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709637	709637	.	+	.	ID=4581;Variant_seq=G;Dbxref=dbSNP_129:rs18995959;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709643	709643	.	+	.	ID=4582;Variant_seq=G;Dbxref=dbSNP_129:rs18995969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709651	709651	.	+	.	ID=4583;Variant_seq=A;Dbxref=dbSNP_129:rs18995989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709656	709656	.	+	.	ID=4584;Variant_seq=A;Dbxref=dbSNP_129:rs18995999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709657	709657	.	+	.	ID=4585;Variant_seq=T;Dbxref=dbSNP_129:rs18996009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709658	709658	.	+	.	ID=4586;Variant_seq=A;Dbxref=dbSNP_129:rs18996019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709667	709667	.	+	.	ID=4587;Variant_seq=G;Dbxref=dbSNP_129:rs18996049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709668	709668	.	+	.	ID=4588;Variant_seq=T;Dbxref=dbSNP_129:rs18996059;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709671	709671	.	+	.	ID=4589;Variant_seq=G;Dbxref=dbSNP_129:rs18996069;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709681	709681	.	+	.	ID=4590;Variant_seq=C;Dbxref=dbSNP_129:rs18996089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709684	709684	.	+	.	ID=4591;Variant_seq=T;Dbxref=dbSNP_129:rs18996099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709688	709688	.	+	.	ID=4592;Variant_seq=A;Dbxref=dbSNP_129:rs18996119;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709690	709690	.	+	.	ID=4593;Variant_seq=C;Dbxref=dbSNP_129:rs18996129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709694	709694	.	+	.	ID=4594;Variant_seq=C;Dbxref=dbSNP_129:rs18996139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709695	709695	.	+	.	ID=4595;Variant_seq=G;Dbxref=dbSNP_129:rs18996149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709707	709707	.	+	.	ID=4596;Variant_seq=G;Dbxref=dbSNP_129:rs18996159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709708	709708	.	+	.	ID=4597;Variant_seq=G;Dbxref=dbSNP_129:rs18996169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709712	709712	.	+	.	ID=4598;Variant_seq=G;Dbxref=dbSNP_129:rs18996199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709713	709713	.	+	.	ID=4599;Variant_seq=A;Dbxref=dbSNP_129:rs18996209;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709716	709716	.	+	.	ID=4600;Variant_seq=G;Dbxref=dbSNP_129:rs18996219;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709808	709808	.	+	.	ID=4601;Variant_seq=G;Dbxref=dbSNP_129:rs18996608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709810	709810	.	+	.	ID=4602;Variant_seq=G;Dbxref=dbSNP_129:rs18996618;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709811	709811	.	+	.	ID=4603;Variant_seq=G;Dbxref=dbSNP_129:rs18996628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709818	709818	.	+	.	ID=4604;Variant_seq=G;Dbxref=dbSNP_129:rs18996648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709823	709823	.	+	.	ID=4605;Variant_seq=G;Dbxref=dbSNP_129:rs18996668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709827	709827	.	+	.	ID=4606;Variant_seq=C;Dbxref=dbSNP_129:rs18996678;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709832	709832	.	+	.	ID=4607;Variant_seq=T;Dbxref=dbSNP_129:rs18996728;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709846	709846	.	+	.	ID=4608;Variant_seq=T;Dbxref=dbSNP_129:rs18996738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709847	709847	.	+	.	ID=4609;Variant_seq=C;Dbxref=dbSNP_129:rs18996748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709849	709849	.	+	.	ID=4610;Variant_seq=A;Dbxref=dbSNP_129:rs18996758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709851	709851	.	+	.	ID=4611;Variant_seq=C;Dbxref=dbSNP_129:rs18996768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709856	709856	.	+	.	ID=4612;Variant_seq=T;Dbxref=dbSNP_129:rs18996788;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709859	709859	.	+	.	ID=4613;Variant_seq=T;Dbxref=dbSNP_129:rs18996798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709860	709860	.	+	.	ID=4614;Variant_seq=T;Dbxref=dbSNP_129:rs18996808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709861	709861	.	+	.	ID=4615;Variant_seq=T;Dbxref=dbSNP_129:rs18996818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709862	709862	.	+	.	ID=4616;Variant_seq=G;Dbxref=dbSNP_129:rs18996828;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709869	709869	.	+	.	ID=4617;Variant_seq=T;Dbxref=dbSNP_129:rs18996858;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709872	709872	.	+	.	ID=4618;Variant_seq=G;Dbxref=dbSNP_129:rs18996868;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709874	709874	.	+	.	ID=4619;Variant_seq=A;Dbxref=dbSNP_129:rs18996878;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709883	709883	.	+	.	ID=4620;Variant_seq=T;Dbxref=dbSNP_129:rs18996918;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709884	709884	.	+	.	ID=4621;Variant_seq=T;Dbxref=dbSNP_129:rs18996928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709892	709892	.	+	.	ID=4622;Variant_seq=C;Dbxref=dbSNP_129:rs18996948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709894	709894	.	+	.	ID=4623;Variant_seq=A;Dbxref=dbSNP_129:rs18996958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709904	709904	.	+	.	ID=4624;Variant_seq=T;Dbxref=dbSNP_129:rs18996978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709905	709905	.	+	.	ID=4625;Variant_seq=T;Dbxref=dbSNP_129:rs18996988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709907	709907	.	+	.	ID=4626;Variant_seq=C;Dbxref=dbSNP_129:rs18996998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709908	709908	.	+	.	ID=4627;Variant_seq=C;Dbxref=dbSNP_129:rs18997008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709911	709911	.	+	.	ID=4628;Variant_seq=C;Dbxref=dbSNP_129:rs18997018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709916	709916	.	+	.	ID=4629;Variant_seq=A;Dbxref=dbSNP_129:rs18997058;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709918	709918	.	+	.	ID=4630;Variant_seq=C;Dbxref=dbSNP_129:rs18997068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709920	709920	.	+	.	ID=4631;Variant_seq=A;Dbxref=dbSNP_129:rs18997078;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709921	709921	.	+	.	ID=4632;Variant_seq=T;Dbxref=dbSNP_129:rs18997088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709923	709923	.	+	.	ID=4633;Variant_seq=G;Dbxref=dbSNP_129:rs18997098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709928	709928	.	+	.	ID=4634;Variant_seq=T;Dbxref=dbSNP_129:rs18997130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709930	709930	.	+	.	ID=4635;Variant_seq=C;Dbxref=dbSNP_129:rs18997140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709932	709932	.	+	.	ID=4636;Variant_seq=C;Dbxref=dbSNP_129:rs18997150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709933	709933	.	+	.	ID=4637;Variant_seq=G;Dbxref=dbSNP_129:rs18997160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709934	709934	.	+	.	ID=4638;Variant_seq=T;Dbxref=dbSNP_129:rs18997170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709935	709935	.	+	.	ID=4639;Variant_seq=T;Dbxref=dbSNP_129:rs18997180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709940	709940	.	+	.	ID=4640;Variant_seq=C;Dbxref=dbSNP_129:rs18997200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709941	709941	.	+	.	ID=4641;Variant_seq=G;Dbxref=dbSNP_129:rs18997210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709944	709944	.	+	.	ID=4642;Variant_seq=T;Dbxref=dbSNP_129:rs18997220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709945	709945	.	+	.	ID=4643;Variant_seq=T;Dbxref=dbSNP_129:rs18997230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709947	709947	.	+	.	ID=4644;Variant_seq=T;Dbxref=dbSNP_129:rs18997240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	709952	709952	.	+	.	ID=4645;Variant_seq=T;Dbxref=dbSNP_129:rs18997260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709956	709956	.	+	.	ID=4646;Variant_seq=T;Dbxref=dbSNP_129:rs18997270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709957	709957	.	+	.	ID=4647;Variant_seq=T;Dbxref=dbSNP_129:rs18997280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709959	709959	.	+	.	ID=4648;Variant_seq=G;Dbxref=dbSNP_129:rs18997290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709964	709964	.	+	.	ID=4649;Variant_seq=G;Dbxref=dbSNP_129:rs18997320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709965	709965	.	+	.	ID=4650;Variant_seq=G;Dbxref=dbSNP_129:rs18997330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	709966	709966	.	+	.	ID=4651;Variant_seq=G;Dbxref=dbSNP_129:rs18997340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709969	709969	.	+	.	ID=4652;Variant_seq=G;Dbxref=dbSNP_129:rs18997350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709976	709976	.	+	.	ID=4653;Variant_seq=C;Dbxref=dbSNP_129:rs18997390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709977	709977	.	+	.	ID=4654;Variant_seq=C;Dbxref=dbSNP_129:rs18997400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709979	709979	.	+	.	ID=4655;Variant_seq=T;Dbxref=dbSNP_129:rs18997410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709982	709982	.	+	.	ID=4656;Variant_seq=C;Dbxref=dbSNP_129:rs18997420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	709983	709983	.	+	.	ID=4657;Variant_seq=T;Dbxref=dbSNP_129:rs18997430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	709990	709990	.	+	.	ID=4658;Variant_seq=A;Dbxref=dbSNP_129:rs18997470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710002	710002	.	+	.	ID=4659;Variant_seq=A;Dbxref=dbSNP_129:rs18997500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710012	710012	.	+	.	ID=4660;Variant_seq=T;Dbxref=dbSNP_129:rs18997530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710013	710013	.	+	.	ID=4661;Variant_seq=T;Dbxref=dbSNP_129:rs18997540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710016	710016	.	+	.	ID=4662;Variant_seq=A;Dbxref=dbSNP_129:rs18997550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710017	710017	.	+	.	ID=4663;Variant_seq=A;Dbxref=dbSNP_129:rs18997560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710024	710024	.	+	.	ID=4664;Variant_seq=A;Dbxref=dbSNP_129:rs18997580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710027	710027	.	+	.	ID=4665;Variant_seq=A;Dbxref=dbSNP_129:rs18997590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710028	710028	.	+	.	ID=4666;Variant_seq=A;Dbxref=dbSNP_129:rs18997600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710031	710031	.	+	.	ID=4667;Variant_seq=T;Dbxref=dbSNP_129:rs18997610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710036	710036	.	+	.	ID=4668;Variant_seq=A;Dbxref=dbSNP_129:rs18997630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710038	710038	.	+	.	ID=4669;Variant_seq=T;Dbxref=dbSNP_129:rs18997640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710048	710048	.	+	.	ID=4670;Variant_seq=T;Dbxref=dbSNP_129:rs18997660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710052	710052	.	+	.	ID=4671;Variant_seq=T;Dbxref=dbSNP_129:rs18997670;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710055	710055	.	+	.	ID=4672;Variant_seq=G;Dbxref=dbSNP_129:rs18997680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710061	710061	.	+	.	ID=4673;Variant_seq=T;Dbxref=dbSNP_129:rs18997700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710067	710067	.	+	.	ID=4674;Variant_seq=G;Dbxref=dbSNP_129:rs18997710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710070	710070	.	+	.	ID=4675;Variant_seq=G;Dbxref=dbSNP_129:rs18997730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710079	710079	.	+	.	ID=4676;Variant_seq=A;Dbxref=dbSNP_129:rs18997740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710084	710084	.	+	.	ID=4677;Variant_seq=T;Dbxref=dbSNP_129:rs18997770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710088	710088	.	+	.	ID=4678;Variant_seq=T;Dbxref=dbSNP_129:rs18997780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710090	710090	.	+	.	ID=4679;Variant_seq=T;Dbxref=dbSNP_129:rs18997790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710091	710091	.	+	.	ID=4680;Variant_seq=A;Dbxref=dbSNP_129:rs18997800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710097	710097	.	+	.	ID=4681;Variant_seq=A;Dbxref=dbSNP_129:rs18997830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710100	710100	.	+	.	ID=4682;Variant_seq=A;Dbxref=dbSNP_129:rs18997840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710108	710108	.	+	.	ID=4683;Variant_seq=G;Dbxref=dbSNP_129:rs18997890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710112	710112	.	+	.	ID=4684;Variant_seq=G;Dbxref=dbSNP_129:rs18997900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710115	710115	.	+	.	ID=4685;Variant_seq=T;Dbxref=dbSNP_129:rs18997910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710116	710116	.	+	.	ID=4686;Variant_seq=T;Dbxref=dbSNP_129:rs18997920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710121	710121	.	+	.	ID=4687;Variant_seq=C;Dbxref=dbSNP_129:rs18997930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710122	710122	.	+	.	ID=4688;Variant_seq=G;Dbxref=dbSNP_129:rs18997940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710124	710124	.	+	.	ID=4689;Variant_seq=T;Dbxref=dbSNP_129:rs18997950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710125	710125	.	+	.	ID=4690;Variant_seq=C;Dbxref=dbSNP_129:rs18997960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710133	710133	.	+	.	ID=4691;Variant_seq=G;Dbxref=dbSNP_129:rs18997980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710139	710139	.	+	.	ID=4692;Variant_seq=T;Dbxref=dbSNP_129:rs18997990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710150	710150	.	+	.	ID=4693;Variant_seq=T;Dbxref=dbSNP_129:rs18998020;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710155	710155	.	+	.	ID=4694;Variant_seq=A;Dbxref=dbSNP_129:rs18998050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710156	710156	.	+	.	ID=4695;Variant_seq=G;Dbxref=dbSNP_129:rs18998060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710158	710158	.	+	.	ID=4696;Variant_seq=T;Dbxref=dbSNP_129:rs18998070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710159	710159	.	+	.	ID=4697;Variant_seq=A;Dbxref=dbSNP_129:rs18998080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710160	710160	.	+	.	ID=4698;Variant_seq=A;Dbxref=dbSNP_129:rs18998090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710164	710164	.	+	.	ID=4699;Variant_seq=G;Dbxref=dbSNP_129:rs18998100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710170	710170	.	+	.	ID=4700;Variant_seq=A;Dbxref=dbSNP_129:rs18998130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710174	710174	.	+	.	ID=4701;Variant_seq=G;Dbxref=dbSNP_129:rs18998140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710182	710182	.	+	.	ID=4702;Variant_seq=T;Dbxref=dbSNP_129:rs18998180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710183	710183	.	+	.	ID=4703;Variant_seq=A;Dbxref=dbSNP_129:rs18998190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710184	710184	.	+	.	ID=4704;Variant_seq=A;Dbxref=dbSNP_129:rs18998200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710185	710185	.	+	.	ID=4705;Variant_seq=A;Dbxref=dbSNP_129:rs18998210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710192	710192	.	+	.	ID=4706;Variant_seq=A;Dbxref=dbSNP_129:rs18998240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710193	710193	.	+	.	ID=4707;Variant_seq=T;Dbxref=dbSNP_129:rs18998250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710196	710196	.	+	.	ID=4708;Variant_seq=T;Dbxref=dbSNP_129:rs18998260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710197	710197	.	+	.	ID=4709;Variant_seq=C;Dbxref=dbSNP_129:rs18998270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710198	710198	.	+	.	ID=4710;Variant_seq=T;Dbxref=dbSNP_129:rs18998280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710204	710204	.	+	.	ID=4711;Variant_seq=T;Dbxref=dbSNP_129:rs18998310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710205	710205	.	+	.	ID=4712;Variant_seq=A;Dbxref=dbSNP_129:rs18998320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710208	710208	.	+	.	ID=4713;Variant_seq=A;Dbxref=dbSNP_129:rs18998330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710209	710209	.	+	.	ID=4714;Variant_seq=A;Dbxref=dbSNP_129:rs18998340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710210	710210	.	+	.	ID=4715;Variant_seq=T;Dbxref=dbSNP_129:rs18998350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710211	710211	.	+	.	ID=4716;Variant_seq=A;Dbxref=dbSNP_129:rs18998360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710215	710215	.	+	.	ID=4717;Variant_seq=A;Dbxref=dbSNP_129:rs18998370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710219	710219	.	+	.	ID=4718;Variant_seq=G;Dbxref=dbSNP_129:rs18998380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710220	710220	.	+	.	ID=4719;Variant_seq=A;Dbxref=dbSNP_129:rs18998390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710221	710221	.	+	.	ID=4720;Variant_seq=T;Dbxref=dbSNP_129:rs18998400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710222	710222	.	+	.	ID=4721;Variant_seq=T;Dbxref=dbSNP_129:rs18998410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710223	710223	.	+	.	ID=4722;Variant_seq=T;Dbxref=dbSNP_129:rs18998420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710226	710226	.	+	.	ID=4723;Variant_seq=T;Dbxref=dbSNP_129:rs18998440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710229	710229	.	+	.	ID=4724;Variant_seq=T;Dbxref=dbSNP_129:rs18998450;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710231	710231	.	+	.	ID=4725;Variant_seq=C;Dbxref=dbSNP_129:rs18998460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710232	710232	.	+	.	ID=4726;Variant_seq=T;Dbxref=dbSNP_129:rs18998470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710233	710233	.	+	.	ID=4727;Variant_seq=T;Dbxref=dbSNP_129:rs18998480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710235	710235	.	+	.	ID=4728;Variant_seq=T;Dbxref=dbSNP_129:rs18998490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710245	710245	.	+	.	ID=4729;Variant_seq=C;Dbxref=dbSNP_129:rs18998520;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710246	710246	.	+	.	ID=4730;Variant_seq=C;Dbxref=dbSNP_129:rs18998530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710251	710251	.	+	.	ID=4731;Variant_seq=A;Dbxref=dbSNP_129:rs18998550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710253	710253	.	+	.	ID=4732;Variant_seq=A;Dbxref=dbSNP_129:rs18998560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710258	710258	.	+	.	ID=4733;Variant_seq=A;Dbxref=dbSNP_129:rs18998570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710260	710260	.	+	.	ID=4734;Variant_seq=T;Dbxref=dbSNP_129:rs18998580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710262	710262	.	+	.	ID=4735;Variant_seq=A;Dbxref=dbSNP_129:rs18998590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710263	710263	.	+	.	ID=4736;Variant_seq=A;Dbxref=dbSNP_129:rs18998600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710266	710266	.	+	.	ID=4737;Variant_seq=A;Dbxref=dbSNP_129:rs18998610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710269	710269	.	+	.	ID=4738;Variant_seq=T;Dbxref=dbSNP_129:rs18998620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710278	710278	.	+	.	ID=4739;Variant_seq=T;Dbxref=dbSNP_129:rs18998650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710279	710279	.	+	.	ID=4740;Variant_seq=T;Dbxref=dbSNP_129:rs18998660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710283	710283	.	+	.	ID=4741;Variant_seq=A;Dbxref=dbSNP_129:rs18998670;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710285	710285	.	+	.	ID=4742;Variant_seq=A;Dbxref=dbSNP_129:rs18998680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710290	710290	.	+	.	ID=4743;Variant_seq=C;Dbxref=dbSNP_129:rs18998700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710296	710296	.	+	.	ID=4744;Variant_seq=T;Dbxref=dbSNP_129:rs18998710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710301	710301	.	+	.	ID=4745;Variant_seq=G;Dbxref=dbSNP_129:rs18998730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710305	710305	.	+	.	ID=4746;Variant_seq=C;Dbxref=dbSNP_129:rs18998740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710307	710307	.	+	.	ID=4747;Variant_seq=G;Dbxref=dbSNP_129:rs18998750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710312	710312	.	+	.	ID=4748;Variant_seq=C;Dbxref=dbSNP_129:rs18998780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710313	710313	.	+	.	ID=4749;Variant_seq=G;Dbxref=dbSNP_129:rs18998790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710318	710318	.	+	.	ID=4750;Variant_seq=G;Dbxref=dbSNP_129:rs18998800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710319	710319	.	+	.	ID=4751;Variant_seq=G;Dbxref=dbSNP_129:rs18998810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710320	710320	.	+	.	ID=4752;Variant_seq=A;Dbxref=dbSNP_129:rs18998820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710322	710322	.	+	.	ID=4753;Variant_seq=G;Dbxref=dbSNP_129:rs18998840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710325	710325	.	+	.	ID=4754;Variant_seq=T;Dbxref=dbSNP_129:rs18998850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710327	710327	.	+	.	ID=4755;Variant_seq=G;Dbxref=dbSNP_129:rs18998860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710328	710328	.	+	.	ID=4756;Variant_seq=G;Dbxref=dbSNP_129:rs18998870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710339	710339	.	+	.	ID=4757;Variant_seq=G;Dbxref=dbSNP_129:rs18998880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710341	710341	.	+	.	ID=4758;Variant_seq=C;Dbxref=dbSNP_129:rs18998890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710342	710342	.	+	.	ID=4759;Variant_seq=G;Dbxref=dbSNP_129:rs18998900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710343	710343	.	+	.	ID=4760;Variant_seq=T;Dbxref=dbSNP_129:rs18998910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710348	710348	.	+	.	ID=4761;Variant_seq=G;Dbxref=dbSNP_129:rs18998920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710349	710349	.	+	.	ID=4762;Variant_seq=G;Dbxref=dbSNP_129:rs18998930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710351	710351	.	+	.	ID=4763;Variant_seq=A;Dbxref=dbSNP_129:rs18998940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710354	710354	.	+	.	ID=4764;Variant_seq=A;Dbxref=dbSNP_129:rs18998950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710355	710355	.	+	.	ID=4765;Variant_seq=A;Dbxref=dbSNP_129:rs18998960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710356	710356	.	+	.	ID=4766;Variant_seq=G;Dbxref=dbSNP_129:rs18998970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710358	710358	.	+	.	ID=4767;Variant_seq=A;Dbxref=dbSNP_129:rs18998990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710359	710359	.	+	.	ID=4768;Variant_seq=T;Dbxref=dbSNP_129:rs18999000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710361	710361	.	+	.	ID=4769;Variant_seq=G;Dbxref=dbSNP_129:rs18999010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710367	710367	.	+	.	ID=4770;Variant_seq=G;Dbxref=dbSNP_129:rs18999020;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710374	710374	.	+	.	ID=4771;Variant_seq=T;Dbxref=dbSNP_129:rs18999040;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710376	710376	.	+	.	ID=4772;Variant_seq=C;Dbxref=dbSNP_129:rs18999050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710379	710379	.	+	.	ID=4773;Variant_seq=G;Dbxref=dbSNP_129:rs18999060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710383	710383	.	+	.	ID=4774;Variant_seq=T;Dbxref=dbSNP_129:rs18999070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710384	710384	.	+	.	ID=4775;Variant_seq=G;Dbxref=dbSNP_129:rs18999080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710396	710396	.	+	.	ID=4776;Variant_seq=C;Dbxref=dbSNP_129:rs18999090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710399	710399	.	+	.	ID=4777;Variant_seq=T;Dbxref=dbSNP_129:rs18999100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710400	710400	.	+	.	ID=4778;Variant_seq=A;Dbxref=dbSNP_129:rs18999110;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710403	710403	.	+	.	ID=4779;Variant_seq=G;Dbxref=dbSNP_129:rs18999120;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710405	710405	.	+	.	ID=4780;Variant_seq=A;Dbxref=dbSNP_129:rs18999130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710411	710411	.	+	.	ID=4781;Variant_seq=G;Dbxref=dbSNP_129:rs18999140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710412	710412	.	+	.	ID=4782;Variant_seq=G;Dbxref=dbSNP_129:rs18999150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710413	710413	.	+	.	ID=4783;Variant_seq=C;Dbxref=dbSNP_129:rs18999160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710415	710415	.	+	.	ID=4784;Variant_seq=T;Dbxref=dbSNP_129:rs18999170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710424	710424	.	+	.	ID=4785;Variant_seq=G;Dbxref=dbSNP_129:rs18999180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710425	710425	.	+	.	ID=4786;Variant_seq=A;Dbxref=dbSNP_129:rs18999190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710426	710426	.	+	.	ID=4787;Variant_seq=A;Dbxref=dbSNP_129:rs18999200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710427	710427	.	+	.	ID=4788;Variant_seq=T;Dbxref=dbSNP_129:rs18999210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710429	710429	.	+	.	ID=4789;Variant_seq=G;Dbxref=dbSNP_129:rs18999220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710432	710432	.	+	.	ID=4790;Variant_seq=A;Dbxref=dbSNP_129:rs18999240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710433	710433	.	+	.	ID=4791;Variant_seq=G;Dbxref=dbSNP_129:rs18999250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710434	710434	.	+	.	ID=4792;Variant_seq=T;Dbxref=dbSNP_129:rs18999260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710437	710437	.	+	.	ID=4793;Variant_seq=T;Dbxref=dbSNP_129:rs18999270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710438	710438	.	+	.	ID=4794;Variant_seq=T;Dbxref=dbSNP_129:rs18999280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710439	710439	.	+	.	ID=4795;Variant_seq=G;Dbxref=dbSNP_129:rs18999290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710441	710441	.	+	.	ID=4796;Variant_seq=G;Dbxref=dbSNP_129:rs18999300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710444	710444	.	+	.	ID=4797;Variant_seq=T;Dbxref=dbSNP_129:rs18999320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710446	710446	.	+	.	ID=4798;Variant_seq=T;Dbxref=dbSNP_129:rs18999330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710449	710449	.	+	.	ID=4799;Variant_seq=G;Dbxref=dbSNP_129:rs18999340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710450	710450	.	+	.	ID=4800;Variant_seq=C;Dbxref=dbSNP_129:rs18999350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710458	710458	.	+	.	ID=4801;Variant_seq=T;Dbxref=dbSNP_129:rs18999380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710462	710462	.	+	.	ID=4802;Variant_seq=C;Dbxref=dbSNP_129:rs18999390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710475	710475	.	+	.	ID=4803;Variant_seq=A;Dbxref=dbSNP_129:rs18999400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710476	710476	.	+	.	ID=4804;Variant_seq=G;Dbxref=dbSNP_129:rs18999410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710480	710480	.	+	.	ID=4805;Variant_seq=G;Dbxref=dbSNP_129:rs18999430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710481	710481	.	+	.	ID=4806;Variant_seq=C;Dbxref=dbSNP_129:rs18999440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710483	710483	.	+	.	ID=4807;Variant_seq=G;Dbxref=dbSNP_129:rs18999450;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710486	710486	.	+	.	ID=4808;Variant_seq=G;Dbxref=dbSNP_129:rs18999460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710488	710488	.	+	.	ID=4809;Variant_seq=G;Dbxref=dbSNP_129:rs18999470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710489	710489	.	+	.	ID=4810;Variant_seq=A;Dbxref=dbSNP_129:rs18999480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710491	710491	.	+	.	ID=4811;Variant_seq=G;Dbxref=dbSNP_129:rs18999490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710497	710497	.	+	.	ID=4812;Variant_seq=G;Dbxref=dbSNP_129:rs18999500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710499	710499	.	+	.	ID=4813;Variant_seq=G;Dbxref=dbSNP_129:rs18999510;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710505	710505	.	+	.	ID=4814;Variant_seq=C;Dbxref=dbSNP_129:rs18999540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710507	710507	.	+	.	ID=4815;Variant_seq=C;Dbxref=dbSNP_129:rs18999550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710508	710508	.	+	.	ID=4816;Variant_seq=G;Dbxref=dbSNP_129:rs18999560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710509	710509	.	+	.	ID=4817;Variant_seq=A;Dbxref=dbSNP_129:rs18999570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710510	710510	.	+	.	ID=4818;Variant_seq=G;Dbxref=dbSNP_129:rs18999580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710517	710517	.	+	.	ID=4819;Variant_seq=A;Dbxref=dbSNP_129:rs18999600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	710519	710519	.	+	.	ID=4820;Variant_seq=A;Dbxref=dbSNP_129:rs18999610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710528	710528	.	+	.	ID=4821;Variant_seq=A;Dbxref=dbSNP_129:rs18999620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710529	710529	.	+	.	ID=4822;Variant_seq=C;Dbxref=dbSNP_129:rs18999630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710531	710531	.	+	.	ID=4823;Variant_seq=C;Dbxref=dbSNP_129:rs18999640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710532	710532	.	+	.	ID=4824;Variant_seq=C;Dbxref=dbSNP_129:rs18999650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710535	710535	.	+	.	ID=4825;Variant_seq=C;Dbxref=dbSNP_129:rs18999660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710541	710541	.	+	.	ID=4826;Variant_seq=A;Dbxref=dbSNP_129:rs18999700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710542	710542	.	+	.	ID=4827;Variant_seq=C;Dbxref=dbSNP_129:rs18999710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710543	710543	.	+	.	ID=4828;Variant_seq=C;Dbxref=dbSNP_129:rs18999720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710545	710545	.	+	.	ID=4829;Variant_seq=C;Dbxref=dbSNP_129:rs18999730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710553	710553	.	+	.	ID=4830;Variant_seq=C;Dbxref=dbSNP_129:rs18999740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710554	710554	.	+	.	ID=4831;Variant_seq=T;Dbxref=dbSNP_129:rs18999750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710557	710557	.	+	.	ID=4832;Variant_seq=C;Dbxref=dbSNP_129:rs18999760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710558	710558	.	+	.	ID=4833;Variant_seq=T;Dbxref=dbSNP_129:rs18999770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710559	710559	.	+	.	ID=4834;Variant_seq=C;Dbxref=dbSNP_129:rs18999780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710564	710564	.	+	.	ID=4835;Variant_seq=A;Dbxref=dbSNP_129:rs18999790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710566	710566	.	+	.	ID=4836;Variant_seq=C;Dbxref=dbSNP_129:rs18999800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710567	710567	.	+	.	ID=4837;Variant_seq=C;Dbxref=dbSNP_129:rs18999810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710568	710568	.	+	.	ID=4838;Variant_seq=C;Dbxref=dbSNP_129:rs18999820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710576	710576	.	+	.	ID=4839;Variant_seq=C;Dbxref=dbSNP_129:rs18999850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710577	710577	.	+	.	ID=4840;Variant_seq=C;Dbxref=dbSNP_129:rs18999860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	710578	710578	.	+	.	ID=4841;Variant_seq=C;Dbxref=dbSNP_129:rs18999870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710579	710579	.	+	.	ID=4842;Variant_seq=G;Dbxref=dbSNP_129:rs18999880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	710821	710821	.	+	.	ID=4843;Variant_seq=C;Dbxref=dbSNP_129:rs18999930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	710903	710903	.	+	.	ID=4844;Variant_seq=A;Dbxref=dbSNP_129:rs18999940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	711380	711380	.	+	.	ID=4845;Variant_seq=C;Dbxref=dbSNP_129:rs19000055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	711819	711819	.	+	.	ID=4846;Variant_seq=A;Dbxref=dbSNP_129:rs19000075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	720567	720567	.	+	.	ID=4847;Variant_seq=C;Dbxref=dbSNP_129:rs19000697;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	721476	721476	.	+	.	ID=4848;Variant_seq=A;Dbxref=dbSNP_129:rs19001051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	721764	721764	.	+	.	ID=4849;Variant_seq=C;Dbxref=dbSNP_129:rs19001091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	724598	724598	.	+	.	ID=4850;Variant_seq=G;Dbxref=dbSNP_129:rs19001284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	725163	725163	.	+	.	ID=4851;Variant_seq=C;Dbxref=dbSNP_129:rs19001405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	734900	734900	.	+	.	ID=4852;Variant_seq=T;Dbxref=dbSNP_129:rs19318225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	736818	736818	.	+	.	ID=4853;Variant_seq=T;Dbxref=dbSNP_129:rs19002046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	737036	737036	.	+	.	ID=4854;Variant_seq=C;Dbxref=dbSNP_129:rs19002054;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	744144	744144	.	+	.	ID=4855;Variant_seq=T;Dbxref=dbSNP_129:rs18198674;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	744261	744261	.	+	.	ID=4856;Variant_seq=A;Dbxref=dbSNP_129:rs19003504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	744715	744715	.	+	.	ID=4857;Variant_seq=T;Dbxref=dbSNP_129:rs18710988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	745240	745240	.	+	.	ID=4858;Variant_seq=C;Dbxref=dbSNP_129:rs19002643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	745348	745348	.	+	.	ID=4859;Variant_seq=A;Dbxref=dbSNP_129:rs52930521;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	745892	745892	.	+	.	ID=4860;Variant_seq=A;Dbxref=dbSNP_129:rs19002689;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	747410	747410	.	+	.	ID=4861;Variant_seq=G;Dbxref=dbSNP_129:rs19002856;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	747829	747829	.	+	.	ID=4862;Variant_seq=T;Dbxref=dbSNP_129:rs18806879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	747897	747897	.	+	.	ID=4863;Variant_seq=C;Dbxref=dbSNP_129:rs19002896;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748194	748194	.	+	.	ID=4864;Variant_seq=G;Dbxref=dbSNP_129:rs18995799;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748197	748197	.	+	.	ID=4865;Variant_seq=A;Dbxref=dbSNP_129:rs18995819;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748198	748198	.	+	.	ID=4866;Variant_seq=G;Dbxref=dbSNP_129:rs18995829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748200	748200	.	+	.	ID=4867;Variant_seq=T;Dbxref=dbSNP_129:rs18995839;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748202	748202	.	+	.	ID=4868;Variant_seq=G;Dbxref=dbSNP_129:rs18995849;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748203	748203	.	+	.	ID=4869;Variant_seq=A;Dbxref=dbSNP_129:rs18995859;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748204	748204	.	+	.	ID=4870;Variant_seq=T;Dbxref=dbSNP_129:rs18995869;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748205	748205	.	+	.	ID=4871;Variant_seq=A;Dbxref=dbSNP_129:rs18995879;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748209	748209	.	+	.	ID=4872;Variant_seq=G;Dbxref=dbSNP_129:rs18995889;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748216	748216	.	+	.	ID=4873;Variant_seq=C;Dbxref=dbSNP_129:rs18995899;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748217	748217	.	+	.	ID=4874;Variant_seq=G;Dbxref=dbSNP_129:rs18995909;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748220	748220	.	+	.	ID=4875;Variant_seq=G;Dbxref=dbSNP_129:rs18995929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748225	748225	.	+	.	ID=4876;Variant_seq=G;Dbxref=dbSNP_129:rs18995939;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748227	748227	.	+	.	ID=4877;Variant_seq=C;Dbxref=dbSNP_129:rs18995949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748230	748230	.	+	.	ID=4878;Variant_seq=G;Dbxref=dbSNP_129:rs18995959;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748236	748236	.	+	.	ID=4879;Variant_seq=G;Dbxref=dbSNP_129:rs18995969;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748244	748244	.	+	.	ID=4880;Variant_seq=A;Dbxref=dbSNP_129:rs18995989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748249	748249	.	+	.	ID=4881;Variant_seq=A;Dbxref=dbSNP_129:rs18995999;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748250	748250	.	+	.	ID=4882;Variant_seq=T;Dbxref=dbSNP_129:rs18996009;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748251	748251	.	+	.	ID=4883;Variant_seq=A;Dbxref=dbSNP_129:rs18996019;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748260	748260	.	+	.	ID=4884;Variant_seq=G;Dbxref=dbSNP_129:rs18996049;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748261	748261	.	+	.	ID=4885;Variant_seq=T;Dbxref=dbSNP_129:rs18996059;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748264	748264	.	+	.	ID=4886;Variant_seq=G;Dbxref=dbSNP_129:rs18996069;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748274	748274	.	+	.	ID=4887;Variant_seq=C;Dbxref=dbSNP_129:rs18996089;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748277	748277	.	+	.	ID=4888;Variant_seq=T;Dbxref=dbSNP_129:rs18996099;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748281	748281	.	+	.	ID=4889;Variant_seq=A;Dbxref=dbSNP_129:rs18996119;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748283	748283	.	+	.	ID=4890;Variant_seq=C;Dbxref=dbSNP_129:rs18996129;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748287	748287	.	+	.	ID=4891;Variant_seq=C;Dbxref=dbSNP_129:rs18996139;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748288	748288	.	+	.	ID=4892;Variant_seq=G;Dbxref=dbSNP_129:rs18996149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748300	748300	.	+	.	ID=4893;Variant_seq=G;Dbxref=dbSNP_129:rs18996159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748301	748301	.	+	.	ID=4894;Variant_seq=G;Dbxref=dbSNP_129:rs18996169;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748305	748305	.	+	.	ID=4895;Variant_seq=G;Dbxref=dbSNP_129:rs18996199;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748306	748306	.	+	.	ID=4896;Variant_seq=A;Dbxref=dbSNP_129:rs18996209;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748309	748309	.	+	.	ID=4897;Variant_seq=G;Dbxref=dbSNP_129:rs18996219;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748402	748402	.	+	.	ID=4898;Variant_seq=G;Dbxref=dbSNP_129:rs18996608;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748404	748404	.	+	.	ID=4899;Variant_seq=G;Dbxref=dbSNP_129:rs18996618;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748405	748405	.	+	.	ID=4900;Variant_seq=G;Dbxref=dbSNP_129:rs18996628;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748412	748412	.	+	.	ID=4901;Variant_seq=G;Dbxref=dbSNP_129:rs18996648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748417	748417	.	+	.	ID=4902;Variant_seq=G;Dbxref=dbSNP_129:rs18996668;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748421	748421	.	+	.	ID=4903;Variant_seq=C;Dbxref=dbSNP_129:rs18996678;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748426	748426	.	+	.	ID=4904;Variant_seq=T;Dbxref=dbSNP_129:rs18996728;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748440	748440	.	+	.	ID=4905;Variant_seq=T;Dbxref=dbSNP_129:rs18996738;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748441	748441	.	+	.	ID=4906;Variant_seq=C;Dbxref=dbSNP_129:rs18996748;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748443	748443	.	+	.	ID=4907;Variant_seq=A;Dbxref=dbSNP_129:rs18996758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748445	748445	.	+	.	ID=4908;Variant_seq=C;Dbxref=dbSNP_129:rs18996768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748450	748450	.	+	.	ID=4909;Variant_seq=T;Dbxref=dbSNP_129:rs18996788;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748453	748453	.	+	.	ID=4910;Variant_seq=T;Dbxref=dbSNP_129:rs18996798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748454	748454	.	+	.	ID=4911;Variant_seq=T;Dbxref=dbSNP_129:rs18996808;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748455	748455	.	+	.	ID=4912;Variant_seq=T;Dbxref=dbSNP_129:rs18996818;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748456	748456	.	+	.	ID=4913;Variant_seq=G;Dbxref=dbSNP_129:rs18996828;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748463	748463	.	+	.	ID=4914;Variant_seq=T;Dbxref=dbSNP_129:rs18996858;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748466	748466	.	+	.	ID=4915;Variant_seq=G;Dbxref=dbSNP_129:rs18996868;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748468	748468	.	+	.	ID=4916;Variant_seq=A;Dbxref=dbSNP_129:rs18996878;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748477	748477	.	+	.	ID=4917;Variant_seq=T;Dbxref=dbSNP_129:rs18996918;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748478	748478	.	+	.	ID=4918;Variant_seq=T;Dbxref=dbSNP_129:rs18996928;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748486	748486	.	+	.	ID=4919;Variant_seq=C;Dbxref=dbSNP_129:rs18996948;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748488	748488	.	+	.	ID=4920;Variant_seq=A;Dbxref=dbSNP_129:rs18996958;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748498	748498	.	+	.	ID=4921;Variant_seq=T;Dbxref=dbSNP_129:rs18996978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748499	748499	.	+	.	ID=4922;Variant_seq=T;Dbxref=dbSNP_129:rs18996988;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748501	748501	.	+	.	ID=4923;Variant_seq=C;Dbxref=dbSNP_129:rs18996998;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748502	748502	.	+	.	ID=4924;Variant_seq=C;Dbxref=dbSNP_129:rs18997008;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748505	748505	.	+	.	ID=4925;Variant_seq=C;Dbxref=dbSNP_129:rs18997018;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748510	748510	.	+	.	ID=4926;Variant_seq=A;Dbxref=dbSNP_129:rs18997058;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748512	748512	.	+	.	ID=4927;Variant_seq=C;Dbxref=dbSNP_129:rs18997068;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748514	748514	.	+	.	ID=4928;Variant_seq=A;Dbxref=dbSNP_129:rs18997078;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748515	748515	.	+	.	ID=4929;Variant_seq=T;Dbxref=dbSNP_129:rs18997088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748517	748517	.	+	.	ID=4930;Variant_seq=G;Dbxref=dbSNP_129:rs18997098;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748522	748522	.	+	.	ID=4931;Variant_seq=T;Dbxref=dbSNP_129:rs18997130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748524	748524	.	+	.	ID=4932;Variant_seq=C;Dbxref=dbSNP_129:rs18997140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748526	748526	.	+	.	ID=4933;Variant_seq=C;Dbxref=dbSNP_129:rs18997150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748527	748527	.	+	.	ID=4934;Variant_seq=G;Dbxref=dbSNP_129:rs18997160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748528	748528	.	+	.	ID=4935;Variant_seq=T;Dbxref=dbSNP_129:rs18997170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748529	748529	.	+	.	ID=4936;Variant_seq=T;Dbxref=dbSNP_129:rs18997180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748534	748534	.	+	.	ID=4937;Variant_seq=C;Dbxref=dbSNP_129:rs18997200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748535	748535	.	+	.	ID=4938;Variant_seq=G;Dbxref=dbSNP_129:rs18997210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748538	748538	.	+	.	ID=4939;Variant_seq=T;Dbxref=dbSNP_129:rs18997220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748539	748539	.	+	.	ID=4940;Variant_seq=T;Dbxref=dbSNP_129:rs18997230;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748541	748541	.	+	.	ID=4941;Variant_seq=T;Dbxref=dbSNP_129:rs18997240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748546	748546	.	+	.	ID=4942;Variant_seq=T;Dbxref=dbSNP_129:rs18997260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748550	748550	.	+	.	ID=4943;Variant_seq=T;Dbxref=dbSNP_129:rs18997270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748551	748551	.	+	.	ID=4944;Variant_seq=T;Dbxref=dbSNP_129:rs18997280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748553	748553	.	+	.	ID=4945;Variant_seq=G;Dbxref=dbSNP_129:rs18997290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748558	748558	.	+	.	ID=4946;Variant_seq=G;Dbxref=dbSNP_129:rs18997320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748559	748559	.	+	.	ID=4947;Variant_seq=G;Dbxref=dbSNP_129:rs18997330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748560	748560	.	+	.	ID=4948;Variant_seq=G;Dbxref=dbSNP_129:rs18997340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748563	748563	.	+	.	ID=4949;Variant_seq=G;Dbxref=dbSNP_129:rs18997350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748570	748570	.	+	.	ID=4950;Variant_seq=C;Dbxref=dbSNP_129:rs18997390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748571	748571	.	+	.	ID=4951;Variant_seq=C;Dbxref=dbSNP_129:rs18997400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748573	748573	.	+	.	ID=4952;Variant_seq=T;Dbxref=dbSNP_129:rs18997410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748576	748576	.	+	.	ID=4953;Variant_seq=C;Dbxref=dbSNP_129:rs18997420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748577	748577	.	+	.	ID=4954;Variant_seq=T;Dbxref=dbSNP_129:rs18997430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748584	748584	.	+	.	ID=4955;Variant_seq=A;Dbxref=dbSNP_129:rs18997470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748596	748596	.	+	.	ID=4956;Variant_seq=A;Dbxref=dbSNP_129:rs18997500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748606	748606	.	+	.	ID=4957;Variant_seq=T;Dbxref=dbSNP_129:rs18997530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748607	748607	.	+	.	ID=4958;Variant_seq=T;Dbxref=dbSNP_129:rs18997540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748610	748610	.	+	.	ID=4959;Variant_seq=A;Dbxref=dbSNP_129:rs18997550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748611	748611	.	+	.	ID=4960;Variant_seq=A;Dbxref=dbSNP_129:rs18997560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748618	748618	.	+	.	ID=4961;Variant_seq=A;Dbxref=dbSNP_129:rs18997580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748621	748621	.	+	.	ID=4962;Variant_seq=A;Dbxref=dbSNP_129:rs18997590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748622	748622	.	+	.	ID=4963;Variant_seq=A;Dbxref=dbSNP_129:rs18997600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748625	748625	.	+	.	ID=4964;Variant_seq=T;Dbxref=dbSNP_129:rs18997610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748630	748630	.	+	.	ID=4965;Variant_seq=A;Dbxref=dbSNP_129:rs18997630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748632	748632	.	+	.	ID=4966;Variant_seq=T;Dbxref=dbSNP_129:rs18997640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748642	748642	.	+	.	ID=4967;Variant_seq=T;Dbxref=dbSNP_129:rs18997660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748646	748646	.	+	.	ID=4968;Variant_seq=T;Dbxref=dbSNP_129:rs18997670;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748649	748649	.	+	.	ID=4969;Variant_seq=G;Dbxref=dbSNP_129:rs18997680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748655	748655	.	+	.	ID=4970;Variant_seq=T;Dbxref=dbSNP_129:rs18997700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748661	748661	.	+	.	ID=4971;Variant_seq=G;Dbxref=dbSNP_129:rs18997710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748664	748664	.	+	.	ID=4972;Variant_seq=G;Dbxref=dbSNP_129:rs18997730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748673	748673	.	+	.	ID=4973;Variant_seq=A;Dbxref=dbSNP_129:rs18997740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748678	748678	.	+	.	ID=4974;Variant_seq=T;Dbxref=dbSNP_129:rs18997770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748682	748682	.	+	.	ID=4975;Variant_seq=T;Dbxref=dbSNP_129:rs18997780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748684	748684	.	+	.	ID=4976;Variant_seq=T;Dbxref=dbSNP_129:rs18997790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748685	748685	.	+	.	ID=4977;Variant_seq=A;Dbxref=dbSNP_129:rs18997800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748691	748691	.	+	.	ID=4978;Variant_seq=A;Dbxref=dbSNP_129:rs18997830;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748694	748694	.	+	.	ID=4979;Variant_seq=A;Dbxref=dbSNP_129:rs18997840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748702	748702	.	+	.	ID=4980;Variant_seq=G;Dbxref=dbSNP_129:rs18997890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748706	748706	.	+	.	ID=4981;Variant_seq=G;Dbxref=dbSNP_129:rs18997900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748709	748709	.	+	.	ID=4982;Variant_seq=T;Dbxref=dbSNP_129:rs18997910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748710	748710	.	+	.	ID=4983;Variant_seq=T;Dbxref=dbSNP_129:rs18997920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748715	748715	.	+	.	ID=4984;Variant_seq=C;Dbxref=dbSNP_129:rs18997930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748716	748716	.	+	.	ID=4985;Variant_seq=G;Dbxref=dbSNP_129:rs18997940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748718	748718	.	+	.	ID=4986;Variant_seq=T;Dbxref=dbSNP_129:rs18997950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748719	748719	.	+	.	ID=4987;Variant_seq=C;Dbxref=dbSNP_129:rs18997960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748727	748727	.	+	.	ID=4988;Variant_seq=G;Dbxref=dbSNP_129:rs18997980;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748733	748733	.	+	.	ID=4989;Variant_seq=T;Dbxref=dbSNP_129:rs18997990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748744	748744	.	+	.	ID=4990;Variant_seq=T;Dbxref=dbSNP_129:rs18998020;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748749	748749	.	+	.	ID=4991;Variant_seq=A;Dbxref=dbSNP_129:rs18998050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748750	748750	.	+	.	ID=4992;Variant_seq=G;Dbxref=dbSNP_129:rs18998060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748752	748752	.	+	.	ID=4993;Variant_seq=T;Dbxref=dbSNP_129:rs18998070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748753	748753	.	+	.	ID=4994;Variant_seq=A;Dbxref=dbSNP_129:rs18998080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748754	748754	.	+	.	ID=4995;Variant_seq=A;Dbxref=dbSNP_129:rs18998090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748758	748758	.	+	.	ID=4996;Variant_seq=G;Dbxref=dbSNP_129:rs18998100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748764	748764	.	+	.	ID=4997;Variant_seq=A;Dbxref=dbSNP_129:rs18998130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748768	748768	.	+	.	ID=4998;Variant_seq=G;Dbxref=dbSNP_129:rs18998140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748776	748776	.	+	.	ID=4999;Variant_seq=T;Dbxref=dbSNP_129:rs18998180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748777	748777	.	+	.	ID=5000;Variant_seq=A;Dbxref=dbSNP_129:rs18998190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748778	748778	.	+	.	ID=5001;Variant_seq=A;Dbxref=dbSNP_129:rs18998200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748779	748779	.	+	.	ID=5002;Variant_seq=A;Dbxref=dbSNP_129:rs18998210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748786	748786	.	+	.	ID=5003;Variant_seq=A;Dbxref=dbSNP_129:rs18998240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748787	748787	.	+	.	ID=5004;Variant_seq=T;Dbxref=dbSNP_129:rs18998250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748790	748790	.	+	.	ID=5005;Variant_seq=T;Dbxref=dbSNP_129:rs18998260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748791	748791	.	+	.	ID=5006;Variant_seq=C;Dbxref=dbSNP_129:rs18998270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748792	748792	.	+	.	ID=5007;Variant_seq=T;Dbxref=dbSNP_129:rs18998280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748798	748798	.	+	.	ID=5008;Variant_seq=T;Dbxref=dbSNP_129:rs18998310;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748799	748799	.	+	.	ID=5009;Variant_seq=A;Dbxref=dbSNP_129:rs18998320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748802	748802	.	+	.	ID=5010;Variant_seq=A;Dbxref=dbSNP_129:rs18998330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748803	748803	.	+	.	ID=5011;Variant_seq=A;Dbxref=dbSNP_129:rs18998340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748804	748804	.	+	.	ID=5012;Variant_seq=T;Dbxref=dbSNP_129:rs18998350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748805	748805	.	+	.	ID=5013;Variant_seq=A;Dbxref=dbSNP_129:rs18998360;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748809	748809	.	+	.	ID=5014;Variant_seq=A;Dbxref=dbSNP_129:rs18998370;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748813	748813	.	+	.	ID=5015;Variant_seq=G;Dbxref=dbSNP_129:rs18998380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748814	748814	.	+	.	ID=5016;Variant_seq=A;Dbxref=dbSNP_129:rs18998390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748815	748815	.	+	.	ID=5017;Variant_seq=T;Dbxref=dbSNP_129:rs18998400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748816	748816	.	+	.	ID=5018;Variant_seq=T;Dbxref=dbSNP_129:rs18998410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748817	748817	.	+	.	ID=5019;Variant_seq=T;Dbxref=dbSNP_129:rs18998420;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748820	748820	.	+	.	ID=5020;Variant_seq=T;Dbxref=dbSNP_129:rs18998440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748823	748823	.	+	.	ID=5021;Variant_seq=T;Dbxref=dbSNP_129:rs18998450;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748825	748825	.	+	.	ID=5022;Variant_seq=C;Dbxref=dbSNP_129:rs18998460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748826	748826	.	+	.	ID=5023;Variant_seq=T;Dbxref=dbSNP_129:rs18998470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748827	748827	.	+	.	ID=5024;Variant_seq=T;Dbxref=dbSNP_129:rs18998480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748829	748829	.	+	.	ID=5025;Variant_seq=T;Dbxref=dbSNP_129:rs18998490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748839	748839	.	+	.	ID=5026;Variant_seq=C;Dbxref=dbSNP_129:rs18998520;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748840	748840	.	+	.	ID=5027;Variant_seq=C;Dbxref=dbSNP_129:rs18998530;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748845	748845	.	+	.	ID=5028;Variant_seq=A;Dbxref=dbSNP_129:rs18998550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748847	748847	.	+	.	ID=5029;Variant_seq=A;Dbxref=dbSNP_129:rs18998560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748852	748852	.	+	.	ID=5030;Variant_seq=A;Dbxref=dbSNP_129:rs18998570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748854	748854	.	+	.	ID=5031;Variant_seq=T;Dbxref=dbSNP_129:rs18998580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748856	748856	.	+	.	ID=5032;Variant_seq=A;Dbxref=dbSNP_129:rs18998590;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748857	748857	.	+	.	ID=5033;Variant_seq=A;Dbxref=dbSNP_129:rs18998600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748860	748860	.	+	.	ID=5034;Variant_seq=A;Dbxref=dbSNP_129:rs18998610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748863	748863	.	+	.	ID=5035;Variant_seq=T;Dbxref=dbSNP_129:rs18998620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748872	748872	.	+	.	ID=5036;Variant_seq=T;Dbxref=dbSNP_129:rs18998650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748873	748873	.	+	.	ID=5037;Variant_seq=T;Dbxref=dbSNP_129:rs18998660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748877	748877	.	+	.	ID=5038;Variant_seq=A;Dbxref=dbSNP_129:rs18998670;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748879	748879	.	+	.	ID=5039;Variant_seq=A;Dbxref=dbSNP_129:rs18998680;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748884	748884	.	+	.	ID=5040;Variant_seq=C;Dbxref=dbSNP_129:rs18998700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748890	748890	.	+	.	ID=5041;Variant_seq=T;Dbxref=dbSNP_129:rs18998710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748895	748895	.	+	.	ID=5042;Variant_seq=G;Dbxref=dbSNP_129:rs18998730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748899	748899	.	+	.	ID=5043;Variant_seq=C;Dbxref=dbSNP_129:rs18998740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748901	748901	.	+	.	ID=5044;Variant_seq=G;Dbxref=dbSNP_129:rs18998750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748906	748906	.	+	.	ID=5045;Variant_seq=C;Dbxref=dbSNP_129:rs18998780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748907	748907	.	+	.	ID=5046;Variant_seq=G;Dbxref=dbSNP_129:rs18998790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748912	748912	.	+	.	ID=5047;Variant_seq=G;Dbxref=dbSNP_129:rs18998800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748913	748913	.	+	.	ID=5048;Variant_seq=G;Dbxref=dbSNP_129:rs18998810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748914	748914	.	+	.	ID=5049;Variant_seq=A;Dbxref=dbSNP_129:rs18998820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748916	748916	.	+	.	ID=5050;Variant_seq=G;Dbxref=dbSNP_129:rs18998840;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748919	748919	.	+	.	ID=5051;Variant_seq=T;Dbxref=dbSNP_129:rs18998850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748921	748921	.	+	.	ID=5052;Variant_seq=G;Dbxref=dbSNP_129:rs18998860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748922	748922	.	+	.	ID=5053;Variant_seq=G;Dbxref=dbSNP_129:rs18998870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748933	748933	.	+	.	ID=5054;Variant_seq=G;Dbxref=dbSNP_129:rs18998880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748935	748935	.	+	.	ID=5055;Variant_seq=C;Dbxref=dbSNP_129:rs18998890;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748936	748936	.	+	.	ID=5056;Variant_seq=G;Dbxref=dbSNP_129:rs18998900;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748937	748937	.	+	.	ID=5057;Variant_seq=T;Dbxref=dbSNP_129:rs18998910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748942	748942	.	+	.	ID=5058;Variant_seq=G;Dbxref=dbSNP_129:rs18998920;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748943	748943	.	+	.	ID=5059;Variant_seq=G;Dbxref=dbSNP_129:rs18998930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748945	748945	.	+	.	ID=5060;Variant_seq=A;Dbxref=dbSNP_129:rs18998940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748948	748948	.	+	.	ID=5061;Variant_seq=A;Dbxref=dbSNP_129:rs18998950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748949	748949	.	+	.	ID=5062;Variant_seq=A;Dbxref=dbSNP_129:rs18998960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748950	748950	.	+	.	ID=5063;Variant_seq=G;Dbxref=dbSNP_129:rs18998970;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748952	748952	.	+	.	ID=5064;Variant_seq=A;Dbxref=dbSNP_129:rs18998990;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748953	748953	.	+	.	ID=5065;Variant_seq=T;Dbxref=dbSNP_129:rs18999000;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748955	748955	.	+	.	ID=5066;Variant_seq=G;Dbxref=dbSNP_129:rs18999010;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748961	748961	.	+	.	ID=5067;Variant_seq=G;Dbxref=dbSNP_129:rs18999020;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748968	748968	.	+	.	ID=5068;Variant_seq=T;Dbxref=dbSNP_129:rs18999040;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748970	748970	.	+	.	ID=5069;Variant_seq=C;Dbxref=dbSNP_129:rs18999050;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748973	748973	.	+	.	ID=5070;Variant_seq=G;Dbxref=dbSNP_129:rs18999060;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748977	748977	.	+	.	ID=5071;Variant_seq=T;Dbxref=dbSNP_129:rs18999070;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748978	748978	.	+	.	ID=5072;Variant_seq=G;Dbxref=dbSNP_129:rs18999080;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748990	748990	.	+	.	ID=5073;Variant_seq=C;Dbxref=dbSNP_129:rs18999090;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	748993	748993	.	+	.	ID=5074;Variant_seq=T;Dbxref=dbSNP_129:rs18999100;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	748994	748994	.	+	.	ID=5075;Variant_seq=A;Dbxref=dbSNP_129:rs18999110;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	748997	748997	.	+	.	ID=5076;Variant_seq=G;Dbxref=dbSNP_129:rs18999120;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	748999	748999	.	+	.	ID=5077;Variant_seq=A;Dbxref=dbSNP_129:rs18999130;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749005	749005	.	+	.	ID=5078;Variant_seq=G;Dbxref=dbSNP_129:rs18999140;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749006	749006	.	+	.	ID=5079;Variant_seq=G;Dbxref=dbSNP_129:rs18999150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749007	749007	.	+	.	ID=5080;Variant_seq=C;Dbxref=dbSNP_129:rs18999160;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749009	749009	.	+	.	ID=5081;Variant_seq=T;Dbxref=dbSNP_129:rs18999170;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749018	749018	.	+	.	ID=5082;Variant_seq=G;Dbxref=dbSNP_129:rs18999180;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749019	749019	.	+	.	ID=5083;Variant_seq=A;Dbxref=dbSNP_129:rs18999190;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749020	749020	.	+	.	ID=5084;Variant_seq=A;Dbxref=dbSNP_129:rs18999200;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749021	749021	.	+	.	ID=5085;Variant_seq=T;Dbxref=dbSNP_129:rs18999210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749023	749023	.	+	.	ID=5086;Variant_seq=G;Dbxref=dbSNP_129:rs18999220;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749026	749026	.	+	.	ID=5087;Variant_seq=A;Dbxref=dbSNP_129:rs18999240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749027	749027	.	+	.	ID=5088;Variant_seq=G;Dbxref=dbSNP_129:rs18999250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749028	749028	.	+	.	ID=5089;Variant_seq=T;Dbxref=dbSNP_129:rs18999260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749031	749031	.	+	.	ID=5090;Variant_seq=T;Dbxref=dbSNP_129:rs18999270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749032	749032	.	+	.	ID=5091;Variant_seq=T;Dbxref=dbSNP_129:rs18999280;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749033	749033	.	+	.	ID=5092;Variant_seq=G;Dbxref=dbSNP_129:rs18999290;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749035	749035	.	+	.	ID=5093;Variant_seq=G;Dbxref=dbSNP_129:rs18999300;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749038	749038	.	+	.	ID=5094;Variant_seq=T;Dbxref=dbSNP_129:rs18999320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749040	749040	.	+	.	ID=5095;Variant_seq=T;Dbxref=dbSNP_129:rs18999330;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749043	749043	.	+	.	ID=5096;Variant_seq=G;Dbxref=dbSNP_129:rs18999340;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749044	749044	.	+	.	ID=5097;Variant_seq=C;Dbxref=dbSNP_129:rs18999350;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749052	749052	.	+	.	ID=5098;Variant_seq=T;Dbxref=dbSNP_129:rs18999380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749056	749056	.	+	.	ID=5099;Variant_seq=C;Dbxref=dbSNP_129:rs18999390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749069	749069	.	+	.	ID=5100;Variant_seq=A;Dbxref=dbSNP_129:rs18999400;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749070	749070	.	+	.	ID=5101;Variant_seq=G;Dbxref=dbSNP_129:rs18999410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749074	749074	.	+	.	ID=5102;Variant_seq=G;Dbxref=dbSNP_129:rs18999430;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749075	749075	.	+	.	ID=5103;Variant_seq=C;Dbxref=dbSNP_129:rs18999440;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749077	749077	.	+	.	ID=5104;Variant_seq=G;Dbxref=dbSNP_129:rs18999450;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749080	749080	.	+	.	ID=5105;Variant_seq=G;Dbxref=dbSNP_129:rs18999460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749082	749082	.	+	.	ID=5106;Variant_seq=G;Dbxref=dbSNP_129:rs18999470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749083	749083	.	+	.	ID=5107;Variant_seq=A;Dbxref=dbSNP_129:rs18999480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749085	749085	.	+	.	ID=5108;Variant_seq=G;Dbxref=dbSNP_129:rs18999490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749091	749091	.	+	.	ID=5109;Variant_seq=G;Dbxref=dbSNP_129:rs18999500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749093	749093	.	+	.	ID=5110;Variant_seq=G;Dbxref=dbSNP_129:rs18999510;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749099	749099	.	+	.	ID=5111;Variant_seq=C;Dbxref=dbSNP_129:rs18999540;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749101	749101	.	+	.	ID=5112;Variant_seq=C;Dbxref=dbSNP_129:rs18999550;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749102	749102	.	+	.	ID=5113;Variant_seq=G;Dbxref=dbSNP_129:rs18999560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749103	749103	.	+	.	ID=5114;Variant_seq=A;Dbxref=dbSNP_129:rs18999570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749104	749104	.	+	.	ID=5115;Variant_seq=G;Dbxref=dbSNP_129:rs18999580;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749111	749111	.	+	.	ID=5116;Variant_seq=A;Dbxref=dbSNP_129:rs18999600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749113	749113	.	+	.	ID=5117;Variant_seq=A;Dbxref=dbSNP_129:rs18999610;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749122	749122	.	+	.	ID=5118;Variant_seq=A;Dbxref=dbSNP_129:rs18999620;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749123	749123	.	+	.	ID=5119;Variant_seq=C;Dbxref=dbSNP_129:rs18999630;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749125	749125	.	+	.	ID=5120;Variant_seq=C;Dbxref=dbSNP_129:rs18999640;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749126	749126	.	+	.	ID=5121;Variant_seq=C;Dbxref=dbSNP_129:rs18999650;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749129	749129	.	+	.	ID=5122;Variant_seq=C;Dbxref=dbSNP_129:rs18999660;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749135	749135	.	+	.	ID=5123;Variant_seq=A;Dbxref=dbSNP_129:rs18999700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749136	749136	.	+	.	ID=5124;Variant_seq=C;Dbxref=dbSNP_129:rs18999710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749137	749137	.	+	.	ID=5125;Variant_seq=C;Dbxref=dbSNP_129:rs18999720;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749139	749139	.	+	.	ID=5126;Variant_seq=C;Dbxref=dbSNP_129:rs18999730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749147	749147	.	+	.	ID=5127;Variant_seq=C;Dbxref=dbSNP_129:rs18999740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749148	749148	.	+	.	ID=5128;Variant_seq=T;Dbxref=dbSNP_129:rs18999750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749151	749151	.	+	.	ID=5129;Variant_seq=C;Dbxref=dbSNP_129:rs18999760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749152	749152	.	+	.	ID=5130;Variant_seq=T;Dbxref=dbSNP_129:rs18999770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749153	749153	.	+	.	ID=5131;Variant_seq=C;Dbxref=dbSNP_129:rs18999780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749158	749158	.	+	.	ID=5132;Variant_seq=A;Dbxref=dbSNP_129:rs18999790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749160	749160	.	+	.	ID=5133;Variant_seq=C;Dbxref=dbSNP_129:rs18999800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749161	749161	.	+	.	ID=5134;Variant_seq=C;Dbxref=dbSNP_129:rs18999810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749162	749162	.	+	.	ID=5135;Variant_seq=C;Dbxref=dbSNP_129:rs18999820;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749170	749170	.	+	.	ID=5136;Variant_seq=C;Dbxref=dbSNP_129:rs18999850;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749171	749171	.	+	.	ID=5137;Variant_seq=C;Dbxref=dbSNP_129:rs18999860;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749172	749172	.	+	.	ID=5138;Variant_seq=C;Dbxref=dbSNP_129:rs18999870;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	749173	749173	.	+	.	ID=5139;Variant_seq=G;Dbxref=dbSNP_129:rs18999880;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	749415	749415	.	+	.	ID=5140;Variant_seq=G;Dbxref=dbSNP_129:rs18999930;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	749497	749497	.	+	.	ID=5141;Variant_seq=G;Dbxref=dbSNP_129:rs18999940;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	749958	749958	.	+	.	ID=5142;Variant_seq=T;Dbxref=dbSNP_129:rs19000055;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	750401	750401	.	+	.	ID=5143;Variant_seq=C;Dbxref=dbSNP_129:rs19000075;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	751451	751451	.	+	.	ID=5144;Variant_seq=T;Dbxref=dbSNP_129:rs19000697;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	752340	752340	.	+	.	ID=5145;Variant_seq=T;Dbxref=dbSNP_129:rs19001051;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	752631	752631	.	+	.	ID=5146;Variant_seq=T;Dbxref=dbSNP_129:rs19001091;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	753696	753696	.	+	.	ID=5147;Variant_seq=A;Dbxref=dbSNP_129:rs19001284;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	754296	754296	.	+	.	ID=5148;Variant_seq=T;Dbxref=dbSNP_129:rs19001405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	755920	755920	.	+	.	ID=5149;Variant_seq=C;Dbxref=dbSNP_129:rs19002046;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	756138	756138	.	+	.	ID=5150;Variant_seq=T;Dbxref=dbSNP_129:rs19002054;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	756647	756647	.	+	.	ID=5151;Variant_seq=T;Dbxref=dbSNP_129:rs19712796;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	756805	756805	.	+	.	ID=5152;Variant_seq=T;Dbxref=dbSNP_129:rs19002949;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	756848	756848	.	+	.	ID=5153;Variant_seq=T;Dbxref=dbSNP_129:rs17972847;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	756850	756850	.	+	.	ID=5154;Variant_seq=A;Dbxref=dbSNP_129:rs19123782;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	758272	758272	.	+	.	ID=5155;Variant_seq=A;Dbxref=dbSNP_129:rs53900341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	758348	758348	.	+	.	ID=5156;Variant_seq=T;Dbxref=dbSNP_129:rs21244910;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	758443	758443	.	+	.	ID=5157;Variant_seq=T;Dbxref=dbSNP_129:rs53486822;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	758444	758444	.	+	.	ID=5158;Variant_seq=A;Dbxref=dbSNP_129:rs54157779;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	758451	758451	.	+	.	ID=5159;Variant_seq=A;Dbxref=dbSNP_129:rs53223979;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	759164	759164	.	+	.	ID=5160;Variant_seq=T;Dbxref=dbSNP_129:rs18199375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	759899	759899	.	+	.	ID=5161;Variant_seq=T;Dbxref=dbSNP_129:rs19003152;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	759909	759909	.	+	.	ID=5162;Variant_seq=T;Dbxref=dbSNP_129:rs17973225;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	759952	759952	.	+	.	ID=5163;Variant_seq=G;Dbxref=dbSNP_129:rs19003159;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	760160	760160	.	+	.	ID=5164;Variant_seq=T;Dbxref=dbSNP_129:rs18199187;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	760403	760403	.	+	.	ID=5165;Variant_seq=G;Dbxref=dbSNP_129:rs19003240;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	760450	760450	.	+	.	ID=5166;Variant_seq=G;Dbxref=dbSNP_129:rs19120987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	761265	761265	.	+	.	ID=5167;Variant_seq=A;Dbxref=dbSNP_129:rs18198926;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	761985	761985	.	+	.	ID=5168;Variant_seq=A;Dbxref=dbSNP_129:rs53604028;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	761993	761993	.	+	.	ID=5169;Variant_seq=C;Dbxref=dbSNP_129:rs52940223;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	762041	762041	.	+	.	ID=5170;Variant_seq=C;Dbxref=dbSNP_129:rs17979117;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	762053	762053	.	+	.	ID=5171;Variant_seq=G;Dbxref=dbSNP_129:rs17979162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	762138	762138	.	+	.	ID=5172;Variant_seq=A;Dbxref=dbSNP_129:rs53748116;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	762147	762147	.	+	.	ID=5173;Variant_seq=G;Dbxref=dbSNP_129:rs54166351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	762150	762150	.	+	.	ID=5174;Variant_seq=A;Dbxref=dbSNP_129:rs53512265;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	762285	762285	.	+	.	ID=5175;Variant_seq=A;Dbxref=dbSNP_129:rs17980053;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	762287	762287	.	+	.	ID=5176;Variant_seq=C;Dbxref=dbSNP_129:rs17980062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	762556	762556	.	+	.	ID=5177;Variant_seq=A;Dbxref=dbSNP_129:rs18199798;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	762770	762770	.	+	.	ID=5178;Variant_seq=G;Dbxref=dbSNP_129:rs19003504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	763608	763608	.	+	.	ID=5179;Variant_seq=A;Dbxref=dbSNP_129:rs19003701;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	763665	763665	.	+	.	ID=5180;Variant_seq=T;Dbxref=dbSNP_129:rs19402345;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	763713	763713	.	+	.	ID=5181;Variant_seq=C;Dbxref=dbSNP_129:rs19002643;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	763936	763936	.	+	.	ID=5182;Variant_seq=T;Dbxref=dbSNP_129:rs18226565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	772062	772062	.	+	.	ID=5183;Variant_seq=T;Dbxref=dbSNP_129:rs19004279;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	773102	773102	.	+	.	ID=5184;Variant_seq=A;Dbxref=dbSNP_129:rs19005724;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	773367	773367	.	+	.	ID=5185;Variant_seq=T;Dbxref=dbSNP_129:rs19441427;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	773930	773930	.	+	.	ID=5186;Variant_seq=T;Dbxref=dbSNP_129:rs21438259;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	774423	774423	.	+	.	ID=5187;Variant_seq=C;Dbxref=dbSNP_129:rs19004512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	775911	775911	.	+	.	ID=5188;Variant_seq=T;Dbxref=dbSNP_129:rs19481989;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	775952	775952	.	+	.	ID=5189;Variant_seq=C;Dbxref=dbSNP_129:rs19481929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	775953	775953	.	+	.	ID=5190;Variant_seq=G;Dbxref=dbSNP_129:rs19481919;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	776001	776001	.	+	.	ID=5191;Variant_seq=T;Dbxref=dbSNP_129:rs19481749;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	776002	776002	.	+	.	ID=5192;Variant_seq=T;Dbxref=dbSNP_129:rs19481739;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	776121	776121	.	+	.	ID=5193;Variant_seq=T;Dbxref=dbSNP_129:rs19481469;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	776133	776133	.	+	.	ID=5194;Variant_seq=C;Dbxref=dbSNP_129:rs19481449;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	776880	776880	.	+	.	ID=5195;Variant_seq=A;Dbxref=dbSNP_129:rs19004767;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	777064	777064	.	+	.	ID=5196;Variant_seq=A;Dbxref=dbSNP_129:rs19004790;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	777569	777569	.	+	.	ID=5197;Variant_seq=G;Dbxref=dbSNP_129:rs19004838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	778841	778841	.	+	.	ID=5198;Variant_seq=T;Dbxref=dbSNP_129:rs53848305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	779128	779128	.	+	.	ID=5199;Variant_seq=T;Dbxref=dbSNP_129:rs18043395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	779178	779178	.	+	.	ID=5200;Variant_seq=G;Dbxref=dbSNP_129:rs54304112;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	780221	780221	.	+	.	ID=5201;Variant_seq=A;Dbxref=dbSNP_129:rs54033088;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	781524	781524	.	+	.	ID=5202;Variant_seq=A;Dbxref=dbSNP_129:rs19005320;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	781874	781874	.	+	.	ID=5203;Variant_seq=G;Dbxref=dbSNP_129:rs19005366;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	782601	782601	.	+	.	ID=5204;Variant_seq=G;Dbxref=dbSNP_129:rs19445511;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	782607	782607	.	+	.	ID=5205;Variant_seq=G;Dbxref=dbSNP_129:rs19445531;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	782628	782628	.	+	.	ID=5206;Variant_seq=A;Dbxref=dbSNP_129:rs19445549;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	783987	783987	.	+	.	ID=5207;Variant_seq=C;Dbxref=dbSNP_129:rs19005724;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	792383	792383	.	+	.	ID=5208;Variant_seq=T;Dbxref=dbSNP_129:rs19006162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	792697	792697	.	+	.	ID=5209;Variant_seq=A;Dbxref=dbSNP_129:rs19006172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	792960	792960	.	+	.	ID=5210;Variant_seq=C;Dbxref=dbSNP_129:rs19006212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	793059	793059	.	+	.	ID=5211;Variant_seq=G;Dbxref=dbSNP_129:rs19006222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	799629	799629	.	+	.	ID=5212;Variant_seq=C;Dbxref=dbSNP_129:rs19006950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	799709	799709	.	+	.	ID=5213;Variant_seq=A;Dbxref=dbSNP_129:rs19006960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	800857	800857	.	+	.	ID=5214;Variant_seq=A;Dbxref=dbSNP_129:rs19006162;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	801171	801171	.	+	.	ID=5215;Variant_seq=C;Dbxref=dbSNP_129:rs19006172;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	801433	801433	.	+	.	ID=5216;Variant_seq=A;Dbxref=dbSNP_129:rs19006212;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	801532	801532	.	+	.	ID=5217;Variant_seq=A;Dbxref=dbSNP_129:rs19006222;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	801911	801911	.	+	.	ID=5218;Variant_seq=C;Dbxref=dbSNP_129:rs19006950;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	801991	801991	.	+	.	ID=5219;Variant_seq=A;Dbxref=dbSNP_129:rs19006960;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	811317	811317	.	+	.	ID=5220;Variant_seq=A;Dbxref=dbSNP_129:rs19007602;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	813773	813773	.	+	.	ID=5221;Variant_seq=A;Dbxref=dbSNP_129:rs19007602;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	835132	835132	.	+	.	ID=5222;Variant_seq=G;Dbxref=dbSNP_129:rs19008663;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	835342	835342	.	+	.	ID=5223;Variant_seq=G;Dbxref=dbSNP_129:rs19008673;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	837408	837408	.	+	.	ID=5224;Variant_seq=A;Dbxref=dbSNP_129:rs19008773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	837438	837438	.	+	.	ID=5225;Variant_seq=T;Dbxref=dbSNP_129:rs19008783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	837512	837512	.	+	.	ID=5226;Variant_seq=G;Dbxref=dbSNP_129:rs19008793;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	837620	837620	.	+	.	ID=5227;Variant_seq=T;Dbxref=dbSNP_129:rs19008813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	837710	837710	.	+	.	ID=5228;Variant_seq=A;Dbxref=dbSNP_129:rs19008823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	838209	838209	.	+	.	ID=5229;Variant_seq=A;Dbxref=dbSNP_129:rs19008843;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	838233	838233	.	+	.	ID=5230;Variant_seq=C;Dbxref=dbSNP_129:rs19008852;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	838349	838349	.	+	.	ID=5231;Variant_seq=T;Dbxref=dbSNP_129:rs19008862;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	838438	838438	.	+	.	ID=5232;Variant_seq=A;Dbxref=dbSNP_129:rs19008882;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	838667	838667	.	+	.	ID=5233;Variant_seq=T;Dbxref=dbSNP_129:rs19008982;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	838788	838788	.	+	.	ID=5234;Variant_seq=T;Dbxref=dbSNP_129:rs19008992;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	838804	838804	.	+	.	ID=5235;Variant_seq=T;Dbxref=dbSNP_129:rs19009012;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	839056	839056	.	+	.	ID=5236;Variant_seq=A;Dbxref=dbSNP_129:rs19009022;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	839450	839450	.	+	.	ID=5237;Variant_seq=A;Dbxref=dbSNP_129:rs19009032;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	839500	839500	.	+	.	ID=5238;Variant_seq=A;Dbxref=dbSNP_129:rs19009042;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	839788	839788	.	+	.	ID=5239;Variant_seq=C;Dbxref=dbSNP_129:rs19009062;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	839855	839855	.	+	.	ID=5240;Variant_seq=C;Dbxref=dbSNP_129:rs19009082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	839991	839991	.	+	.	ID=5241;Variant_seq=T;Dbxref=dbSNP_129:rs19009104;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	839991	839991	.	+	.	ID=5242;Variant_seq=T;Dbxref=dbSNP_129:rs53127403;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	839993	839993	.	+	.	ID=5243;Variant_seq=A;Dbxref=dbSNP_129:rs19009114;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	839993	839993	.	+	.	ID=5244;Variant_seq=A;Dbxref=dbSNP_129:rs54251905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	840033	840033	.	+	.	ID=5245;Variant_seq=A;Dbxref=dbSNP_129:rs19009124;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	840165	840165	.	+	.	ID=5246;Variant_seq=A;Dbxref=dbSNP_129:rs19009134;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	840268	840268	.	+	.	ID=5247;Variant_seq=C;Dbxref=dbSNP_129:rs53341695;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	840373	840373	.	+	.	ID=5248;Variant_seq=T;Dbxref=dbSNP_129:rs19875936;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	840407	840407	.	+	.	ID=5249;Variant_seq=T;Dbxref=dbSNP_129:rs54183657;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	840452	840452	.	+	.	ID=5250;Variant_seq=C;Dbxref=dbSNP_129:rs54287447;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	844646	844646	.	+	.	ID=5251;Variant_seq=A;Dbxref=dbSNP_129:rs53410337;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	844752	844752	.	+	.	ID=5252;Variant_seq=AATAC;Dbxref=dbSNP_129:rs53277056;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	insertion	844799	844799	.	+	.	ID=5253;Variant_seq=TC;Dbxref=dbSNP_129:rs53640662;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	853805	853805	.	+	.	ID=5254;Variant_seq=T;Dbxref=dbSNP_129:rs19010598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	859767	859767	.	+	.	ID=5255;Variant_seq=T;Dbxref=dbSNP_129:rs19011135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	860365	860365	.	+	.	ID=5256;Variant_seq=G;Dbxref=dbSNP_129:rs19011151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	863517	863517	.	+	.	ID=5257;Variant_seq=G;Dbxref=dbSNP_129:rs19010598;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	864709	864709	.	+	.	ID=5258;Variant_seq=G;Dbxref=dbSNP_129:rs19011135;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	865297	865297	.	+	.	ID=5259;Variant_seq=T;Dbxref=dbSNP_129:rs19011151;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	867737	867737	.	+	.	ID=5260;Variant_seq=A;Dbxref=dbSNP_129:rs19011541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	867993	867993	.	+	.	ID=5261;Variant_seq=G;Dbxref=dbSNP_129:rs19011549;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	870285	870285	.	+	.	ID=5262;Variant_seq=AG;Dbxref=dbSNP_129:rs53846464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	deletion	870366	870371	.	+	.	ID=5263;Variant_seq=-;Dbxref=dbSNP_129:rs52869592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AGAGGA
5	dbSNP	SNV	870584	870584	.	+	.	ID=5264;Variant_seq=C;Dbxref=dbSNP_129:rs19011597;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	870884	870884	.	+	.	ID=5265;Variant_seq=T;Dbxref=dbSNP_129:rs19011605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	878623	878623	.	+	.	ID=5266;Variant_seq=T;Dbxref=dbSNP_129:rs21062429;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	878930	878930	.	+	.	ID=5267;Variant_seq=C;Dbxref=dbSNP_129:rs19011955;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	880396	880396	.	+	.	ID=5268;Variant_seq=C;Dbxref=dbSNP_129:rs19012082;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	887866	887866	.	+	.	ID=5269;Variant_seq=A;Dbxref=dbSNP_129:rs18274250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	905024	905024	.	+	.	ID=5270;Variant_seq=G;Dbxref=dbSNP_129:rs19011541;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	905280	905280	.	+	.	ID=5271;Variant_seq=A;Dbxref=dbSNP_129:rs19011549;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	907569	907569	.	+	.	ID=5272;Variant_seq=AG;Dbxref=dbSNP_129:rs53846464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	deletion	907650	907655	.	+	.	ID=5273;Variant_seq=-;Dbxref=dbSNP_129:rs52869592;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=AGAGGA
5	dbSNP	SNV	907868	907868	.	+	.	ID=5274;Variant_seq=G;Dbxref=dbSNP_129:rs19011597;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	908180	908180	.	+	.	ID=5275;Variant_seq=C;Dbxref=dbSNP_129:rs19011605;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	912761	912761	.	+	.	ID=5276;Variant_seq=A;Dbxref=dbSNP_129:rs19013460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	912862	912862	.	+	.	ID=5277;Variant_seq=G;Dbxref=dbSNP_129:rs19013470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	913248	913248	.	+	.	ID=5278;Variant_seq=A;Dbxref=dbSNP_129:rs19013480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	913355	913355	.	+	.	ID=5279;Variant_seq=T;Dbxref=dbSNP_129:rs19013490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	920065	920065	.	+	.	ID=5280;Variant_seq=T;Dbxref=dbSNP_129:rs19013781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	921979	921979	.	+	.	ID=5281;Variant_seq=A;Dbxref=dbSNP_129:rs19013841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	922520	922520	.	+	.	ID=5282;Variant_seq=A;Dbxref=dbSNP_129:rs19013901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	923032	923032	.	+	.	ID=5283;Variant_seq=G;Dbxref=dbSNP_129:rs19013911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	923153	923153	.	+	.	ID=5284;Variant_seq=A;Dbxref=dbSNP_129:rs19013921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	923435	923435	.	+	.	ID=5285;Variant_seq=T;Dbxref=dbSNP_129:rs19013931;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	923804	923804	.	+	.	ID=5286;Variant_seq=C;Dbxref=dbSNP_129:rs19013941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	924397	924397	.	+	.	ID=5287;Variant_seq=C;Dbxref=dbSNP_129:rs19013951;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	924485	924485	.	+	.	ID=5288;Variant_seq=A;Dbxref=dbSNP_129:rs19013961;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	925433	925433	.	+	.	ID=5289;Variant_seq=G;Dbxref=dbSNP_129:rs19013460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	925534	925534	.	+	.	ID=5290;Variant_seq=A;Dbxref=dbSNP_129:rs19013470;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	925920	925920	.	+	.	ID=5291;Variant_seq=G;Dbxref=dbSNP_129:rs19013480;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	926027	926027	.	+	.	ID=5292;Variant_seq=A;Dbxref=dbSNP_129:rs19013490;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	926342	926342	.	+	.	ID=5293;Variant_seq=C;Dbxref=dbSNP_129:rs19013971;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	926363	926363	.	+	.	ID=5294;Variant_seq=G;Dbxref=dbSNP_129:rs19013981;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	926402	926402	.	+	.	ID=5295;Variant_seq=A;Dbxref=dbSNP_129:rs19013991;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	926525	926525	.	+	.	ID=5296;Variant_seq=C;Dbxref=dbSNP_129:rs19014011;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	932499	932499	.	+	.	ID=5297;Variant_seq=C;Dbxref=dbSNP_129:rs19014881;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	932582	932582	.	+	.	ID=5298;Variant_seq=T;Dbxref=dbSNP_129:rs19014901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	942687	942687	.	+	.	ID=5299;Variant_seq=T;Dbxref=dbSNP_129:rs19016472;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	954075	954075	.	+	.	ID=5300;Variant_seq=C;Dbxref=dbSNP_129:rs19016472;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	960292	960292	.	+	.	ID=5301;Variant_seq=T;Dbxref=dbSNP_129:rs19013781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	962944	962944	.	+	.	ID=5302;Variant_seq=C;Dbxref=dbSNP_129:rs19013841;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	963492	963492	.	+	.	ID=5303;Variant_seq=G;Dbxref=dbSNP_129:rs19013901;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	964004	964004	.	+	.	ID=5304;Variant_seq=T;Dbxref=dbSNP_129:rs19013911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	964125	964125	.	+	.	ID=5305;Variant_seq=G;Dbxref=dbSNP_129:rs19013921;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	964407	964407	.	+	.	ID=5306;Variant_seq=T;Dbxref=dbSNP_129:rs19013931;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	964779	964779	.	+	.	ID=5307;Variant_seq=T;Dbxref=dbSNP_129:rs19013941;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	965373	965373	.	+	.	ID=5308;Variant_seq=T;Dbxref=dbSNP_129:rs19013951;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	965461	965461	.	+	.	ID=5309;Variant_seq=G;Dbxref=dbSNP_129:rs19013961;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	966226	966226	.	+	.	ID=5310;Variant_seq=G;Dbxref=dbSNP_129:rs19017690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	967311	967311	.	+	.	ID=5311;Variant_seq=T;Dbxref=dbSNP_129:rs19016962;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	968151	968151	.	+	.	ID=5312;Variant_seq=G;Dbxref=dbSNP_129:rs18735417;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	968180	968180	.	+	.	ID=5313;Variant_seq=A;Dbxref=dbSNP_129:rs18735408;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	968256	968256	.	+	.	ID=5314;Variant_seq=T;Dbxref=dbSNP_129:rs18735390;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	968446	968446	.	+	.	ID=5315;Variant_seq=A;Dbxref=dbSNP_129:rs18735372;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	968462	968462	.	+	.	ID=5316;Variant_seq=T;Dbxref=dbSNP_129:rs18735363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	968545	968545	.	+	.	ID=5317;Variant_seq=T;Dbxref=dbSNP_129:rs18735354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	969261	969261	.	+	.	ID=5318;Variant_seq=A;Dbxref=dbSNP_129:rs54296473;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	969263	969263	.	+	.	ID=5319;Variant_seq=C;Dbxref=dbSNP_129:rs53140829;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	969271	969271	.	+	.	ID=5320;Variant_seq=A;Dbxref=dbSNP_129:rs54063380;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	969275	969275	.	+	.	ID=5321;Variant_seq=A;Dbxref=dbSNP_129:rs53594684;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	969277	969277	.	+	.	ID=5322;Variant_seq=A;Dbxref=dbSNP_129:rs53419768;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	969284	969284	.	+	.	ID=5323;Variant_seq=T;Dbxref=dbSNP_129:rs54234426;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	969311	969311	.	+	.	ID=5324;Variant_seq=T;Dbxref=dbSNP_129:rs53632489;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	969312	969312	.	+	.	ID=5325;Variant_seq=T;Dbxref=dbSNP_129:rs54130773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	969317	969317	.	+	.	ID=5326;Variant_seq=T;Dbxref=dbSNP_129:rs54142289;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	969319	969319	.	+	.	ID=5327;Variant_seq=G;Dbxref=dbSNP_129:rs53377410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971428	971428	.	+	.	ID=5328;Variant_seq=T;Dbxref=dbSNP_129:rs18735264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	971566	971566	.	+	.	ID=5329;Variant_seq=G;Dbxref=dbSNP_129:rs18735255;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971619	971619	.	+	.	ID=5330;Variant_seq=A;Dbxref=dbSNP_129:rs18735246;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	971697	971697	.	+	.	ID=5331;Variant_seq=G;Dbxref=dbSNP_129:rs18735237;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971738	971738	.	+	.	ID=5332;Variant_seq=C;Dbxref=dbSNP_129:rs18735228;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971875	971875	.	+	.	ID=5333;Variant_seq=G;Dbxref=dbSNP_129:rs53033858;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971877	971877	.	+	.	ID=5334;Variant_seq=C;Dbxref=dbSNP_129:rs53068277;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	971889	971889	.	+	.	ID=5335;Variant_seq=A;Dbxref=dbSNP_129:rs52880706;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	971897	971897	.	+	.	ID=5336;Variant_seq=T;Dbxref=dbSNP_129:rs53362208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971900	971900	.	+	.	ID=5337;Variant_seq=C;Dbxref=dbSNP_129:rs53903478;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	971903	971903	.	+	.	ID=5338;Variant_seq=G;Dbxref=dbSNP_129:rs53159113;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971905	971905	.	+	.	ID=5339;Variant_seq=C;Dbxref=dbSNP_129:rs18735219;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	971916	971916	.	+	.	ID=5340;Variant_seq=C;Dbxref=dbSNP_129:rs53588837;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	971917	971917	.	+	.	ID=5341;Variant_seq=C;Dbxref=dbSNP_129:rs53655171;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	971922	971922	.	+	.	ID=5342;Variant_seq=A;Dbxref=dbSNP_129:rs52846065;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	971928	971928	.	+	.	ID=5343;Variant_seq=A;Dbxref=dbSNP_129:rs52846845;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	971931	971931	.	+	.	ID=5344;Variant_seq=T;Dbxref=dbSNP_129:rs52979153;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	971952	971952	.	+	.	ID=5345;Variant_seq=A;Dbxref=dbSNP_129:rs53530600;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	971953	971953	.	+	.	ID=5346;Variant_seq=A;Dbxref=dbSNP_129:rs54093801;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	insertion	971953	971953	.	+	.	ID=5347;Variant_seq=T;Dbxref=dbSNP_129:rs53825484;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	971967	971967	.	+	.	ID=5348;Variant_seq=T;Dbxref=dbSNP_129:rs53805561;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	971968	971968	.	+	.	ID=5349;Variant_seq=A;Dbxref=dbSNP_129:rs53990471;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	971969	971969	.	+	.	ID=5350;Variant_seq=C;Dbxref=dbSNP_129:rs53729472;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	971974	971974	.	+	.	ID=5351;Variant_seq=A;Dbxref=dbSNP_129:rs53302716;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	971982	971982	.	+	.	ID=5352;Variant_seq=A;Dbxref=dbSNP_129:rs53350963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	972017	972017	.	+	.	ID=5353;Variant_seq=G;Dbxref=dbSNP_129:rs53348015;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	972020	972020	.	+	.	ID=5354;Variant_seq=G;Dbxref=dbSNP_129:rs53696897;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	972023	972023	.	+	.	ID=5355;Variant_seq=A;Dbxref=dbSNP_129:rs53570935;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	insertion	972027	972027	.	+	.	ID=5356;Variant_seq=G;Dbxref=dbSNP_129:rs54040322;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	insertion	972029	972029	.	+	.	ID=5357;Variant_seq=CAA;Dbxref=dbSNP_129:rs52852229;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	972040	972040	.	+	.	ID=5358;Variant_seq=A;Dbxref=dbSNP_129:rs18735210;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	972050	972050	.	+	.	ID=5359;Variant_seq=G;Dbxref=dbSNP_129:rs53339500;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	972063	972063	.	+	.	ID=5360;Variant_seq=C;Dbxref=dbSNP_129:rs53018719;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	972065	972065	.	+	.	ID=5361;Variant_seq=G;Dbxref=dbSNP_129:rs53262193;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	972067	972067	.	+	.	ID=5362;Variant_seq=A;Dbxref=dbSNP_129:rs53332375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	972069	972069	.	+	.	ID=5363;Variant_seq=C;Dbxref=dbSNP_129:rs53068150;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	972086	972086	.	+	.	ID=5364;Variant_seq=G;Dbxref=dbSNP_129:rs53415128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	972092	972092	.	+	.	ID=5365;Variant_seq=T;Dbxref=dbSNP_129:rs53516776;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	972096	972096	.	+	.	ID=5366;Variant_seq=T;Dbxref=dbSNP_129:rs54102665;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	972105	972105	.	+	.	ID=5367;Variant_seq=G;Dbxref=dbSNP_129:rs53356363;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	972108	972108	.	+	.	ID=5368;Variant_seq=C;Dbxref=dbSNP_129:rs53442679;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	972113	972113	.	+	.	ID=5369;Variant_seq=G;Dbxref=dbSNP_129:rs52969781;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	972115	972115	.	+	.	ID=5370;Variant_seq=CGGTACGC;Dbxref=dbSNP_129:rs53340543;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	976811	976811	.	+	.	ID=5371;Variant_seq=T;Dbxref=dbSNP_129:rs19017231;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	976849	976849	.	+	.	ID=5372;Variant_seq=A;Dbxref=dbSNP_129:rs19017241;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	976850	976850	.	+	.	ID=5373;Variant_seq=A;Dbxref=dbSNP_129:rs19017251;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	976933	976933	.	+	.	ID=5374;Variant_seq=G;Dbxref=dbSNP_129:rs19017271;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	977245	977245	.	+	.	ID=5375;Variant_seq=C;Dbxref=dbSNP_129:rs19017351;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	980393	980393	.	+	.	ID=5376;Variant_seq=A;Dbxref=dbSNP_129:rs19017690;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	981481	981481	.	+	.	ID=5377;Variant_seq=T;Dbxref=dbSNP_129:rs19016962;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	984321	984321	.	+	.	ID=5378;Variant_seq=T;Dbxref=dbSNP_129:rs19019791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1014986	1014986	.	+	.	ID=5379;Variant_seq=G;Dbxref=dbSNP_129:rs19019011;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1015246	1015246	.	+	.	ID=5380;Variant_seq=C;Dbxref=dbSNP_129:rs19019061;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1026189	1026189	.	+	.	ID=5381;Variant_seq=G;Dbxref=dbSNP_129:rs19019791;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1045506	1045506	.	+	.	ID=5382;Variant_seq=C;Dbxref=dbSNP_129:rs19021264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1045836	1045836	.	+	.	ID=5383;Variant_seq=G;Dbxref=dbSNP_129:rs19021504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1045932	1045932	.	+	.	ID=5384;Variant_seq=A;Dbxref=dbSNP_129:rs19021514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1047364	1047364	.	+	.	ID=5385;Variant_seq=C;Dbxref=dbSNP_129:rs19020464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1047406	1047406	.	+	.	ID=5386;Variant_seq=G;Dbxref=dbSNP_129:rs19020474;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1057465	1057465	.	+	.	ID=5387;Variant_seq=T;Dbxref=dbSNP_129:rs19021264;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1061720	1061720	.	+	.	ID=5388;Variant_seq=A;Dbxref=dbSNP_129:rs19021504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1061816	1061816	.	+	.	ID=5389;Variant_seq=G;Dbxref=dbSNP_129:rs19021514;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1063245	1063245	.	+	.	ID=5390;Variant_seq=T;Dbxref=dbSNP_129:rs19020464;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1063287	1063287	.	+	.	ID=5391;Variant_seq=A;Dbxref=dbSNP_129:rs19020474;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1073984	1073984	.	+	.	ID=5392;Variant_seq=C;Dbxref=dbSNP_129:rs19022512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1074252	1074252	.	+	.	ID=5393;Variant_seq=G;Dbxref=dbSNP_129:rs19022522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1079950	1079950	.	+	.	ID=5394;Variant_seq=T;Dbxref=dbSNP_129:rs19022412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1080013	1080013	.	+	.	ID=5395;Variant_seq=T;Dbxref=dbSNP_129:rs19022412;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1087365	1087365	.	+	.	ID=5396;Variant_seq=A;Dbxref=dbSNP_129:rs19022512;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1087637	1087637	.	+	.	ID=5397;Variant_seq=A;Dbxref=dbSNP_129:rs19022522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1099014	1099014	.	+	.	ID=5398;Variant_seq=T;Dbxref=dbSNP_129:rs19024953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1099154	1099154	.	+	.	ID=5399;Variant_seq=C;Dbxref=dbSNP_129:rs19023454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1099868	1099868	.	+	.	ID=5400;Variant_seq=G;Dbxref=dbSNP_129:rs19023584;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1100958	1100958	.	+	.	ID=5401;Variant_seq=T;Dbxref=dbSNP_129:rs19023803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1101041	1101041	.	+	.	ID=5402;Variant_seq=T;Dbxref=dbSNP_129:rs53276493;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1101155	1101155	.	+	.	ID=5403;Variant_seq=G;Dbxref=dbSNP_129:rs53190576;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1101237	1101237	.	+	.	ID=5404;Variant_seq=G;Dbxref=dbSNP_129:rs53793192;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1101716	1101716	.	+	.	ID=5405;Variant_seq=C;Dbxref=dbSNP_129:rs18831787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1102389	1102389	.	+	.	ID=5406;Variant_seq=T;Dbxref=dbSNP_129:rs19023953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1102402	1102402	.	+	.	ID=5407;Variant_seq=A;Dbxref=dbSNP_129:rs53406671;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1105224	1105224	.	+	.	ID=5408;Variant_seq=A;Dbxref=dbSNP_129:rs20609276;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1105529	1105529	.	+	.	ID=5409;Variant_seq=G;Dbxref=dbSNP_129:rs19024205;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1106614	1106614	.	+	.	ID=5410;Variant_seq=T;Dbxref=dbSNP_129:rs19024444;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	deletion	1107552	1107552	.	+	.	ID=5411;Variant_seq=-;Dbxref=dbSNP_129:rs52920504;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1107554	1107554	.	+	.	ID=5412;Variant_seq=T;Dbxref=dbSNP_129:rs53177911;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1107609	1107609	.	+	.	ID=5413;Variant_seq=T;Dbxref=dbSNP_129:rs19024604;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1107796	1107796	.	+	.	ID=5414;Variant_seq=G;Dbxref=dbSNP_129:rs19024634;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1108001	1108001	.	+	.	ID=5415;Variant_seq=G;Dbxref=dbSNP_129:rs19024654;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1110937	1110937	.	+	.	ID=5416;Variant_seq=T;Dbxref=dbSNP_129:rs19025173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1112445	1112445	.	+	.	ID=5417;Variant_seq=A;Dbxref=dbSNP_129:rs19025944;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1112967	1112967	.	+	.	ID=5418;Variant_seq=G;Dbxref=dbSNP_129:rs19024713;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1112985	1112985	.	+	.	ID=5419;Variant_seq=C;Dbxref=dbSNP_129:rs19024723;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1112993	1112993	.	+	.	ID=5420;Variant_seq=C;Dbxref=dbSNP_129:rs19024733;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1113036	1113036	.	+	.	ID=5421;Variant_seq=G;Dbxref=dbSNP_129:rs19024743;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113063	1113063	.	+	.	ID=5422;Variant_seq=G;Dbxref=dbSNP_129:rs19024753;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113084	1113084	.	+	.	ID=5423;Variant_seq=G;Dbxref=dbSNP_129:rs19024763;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113125	1113125	.	+	.	ID=5424;Variant_seq=A;Dbxref=dbSNP_129:rs19024773;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1113142	1113142	.	+	.	ID=5425;Variant_seq=T;Dbxref=dbSNP_129:rs19024783;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1113178	1113178	.	+	.	ID=5426;Variant_seq=G;Dbxref=dbSNP_129:rs19024803;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113281	1113281	.	+	.	ID=5427;Variant_seq=A;Dbxref=dbSNP_129:rs19024813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1113292	1113292	.	+	.	ID=5428;Variant_seq=A;Dbxref=dbSNP_129:rs19024823;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1113327	1113327	.	+	.	ID=5429;Variant_seq=T;Dbxref=dbSNP_129:rs19024833;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1113408	1113408	.	+	.	ID=5430;Variant_seq=G;Dbxref=dbSNP_129:rs19024853;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113447	1113447	.	+	.	ID=5431;Variant_seq=C;Dbxref=dbSNP_129:rs19024873;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1113515	1113515	.	+	.	ID=5432;Variant_seq=G;Dbxref=dbSNP_129:rs19024893;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113704	1113704	.	+	.	ID=5433;Variant_seq=T;Dbxref=dbSNP_129:rs19024913;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1113797	1113797	.	+	.	ID=5434;Variant_seq=G;Dbxref=dbSNP_129:rs19024923;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1113813	1113813	.	+	.	ID=5435;Variant_seq=A;Dbxref=dbSNP_129:rs19024933;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1113879	1113879	.	+	.	ID=5436;Variant_seq=T;Dbxref=dbSNP_129:rs19024953;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1114019	1114019	.	+	.	ID=5437;Variant_seq=T;Dbxref=dbSNP_129:rs19023454;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1118008	1118008	.	+	.	ID=5438;Variant_seq=G;Dbxref=dbSNP_129:rs19025173;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1126751	1126751	.	+	.	ID=5439;Variant_seq=G;Dbxref=dbSNP_129:rs19025944;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1144394	1144394	.	+	.	ID=5440;Variant_seq=T;Dbxref=dbSNP_129:rs18946208;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1144405	1144405	.	+	.	ID=5441;Variant_seq=T;Dbxref=dbSNP_129:rs19027353;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1163931	1163931	.	+	.	ID=5442;Variant_seq=C;Dbxref=dbSNP_129:rs19029063;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1165128	1165128	.	+	.	ID=5443;Variant_seq=T;Dbxref=dbSNP_129:rs19029262;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1171488	1171488	.	+	.	ID=5444;Variant_seq=G;Dbxref=dbSNP_129:rs19029692;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1171669	1171669	.	+	.	ID=5445;Variant_seq=A;Dbxref=dbSNP_129:rs19029702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1172143	1172143	.	+	.	ID=5446;Variant_seq=A;Dbxref=dbSNP_129:rs53170039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1172517	1172517	.	+	.	ID=5447;Variant_seq=G;Dbxref=dbSNP_129:rs53913460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1172533	1172533	.	+	.	ID=5448;Variant_seq=A;Dbxref=dbSNP_129:rs53338407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	1172768	1172768	.	+	.	ID=5449;Variant_seq=-;Dbxref=dbSNP_129:rs53578560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	1172770	1172770	.	+	.	ID=5450;Variant_seq=-;Dbxref=dbSNP_129:rs53446407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	1172775	1172775	.	+	.	ID=5451;Variant_seq=-;Dbxref=dbSNP_129:rs52955528;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1172777	1172777	.	+	.	ID=5452;Variant_seq=A;Dbxref=dbSNP_129:rs53001813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1172791	1172791	.	+	.	ID=5453;Variant_seq=G;Dbxref=dbSNP_129:rs54385700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1172807	1172807	.	+	.	ID=5454;Variant_seq=C;Dbxref=dbSNP_129:rs53268996;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1172811	1172811	.	+	.	ID=5455;Variant_seq=T;Dbxref=dbSNP_129:rs54357731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1172850	1172850	.	+	.	ID=5456;Variant_seq=T;Dbxref=dbSNP_129:rs54181838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1172896	1172896	.	+	.	ID=5457;Variant_seq=C;Dbxref=dbSNP_129:rs53997495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1172899	1172899	.	+	.	ID=5458;Variant_seq=T;Dbxref=dbSNP_129:rs52926968;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	deletion	1172906	1172909	.	+	.	ID=5459;Variant_seq=-;Dbxref=dbSNP_129:rs53033778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TATA
5	dbSNP	SNV	1174438	1174438	.	+	.	ID=5460;Variant_seq=A;Dbxref=dbSNP_129:rs19029692;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1174619	1174619	.	+	.	ID=5461;Variant_seq=G;Dbxref=dbSNP_129:rs19029702;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1175097	1175097	.	+	.	ID=5462;Variant_seq=A;Dbxref=dbSNP_129:rs53170039;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	1175113	1175113	.	+	.	ID=5463;Variant_seq=-;Dbxref=dbSNP_129:rs53316149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1175707	1175707	.	+	.	ID=5464;Variant_seq=G;Dbxref=dbSNP_129:rs53913460;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1175723	1175723	.	+	.	ID=5465;Variant_seq=A;Dbxref=dbSNP_129:rs53338407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	1175960	1175960	.	+	.	ID=5466;Variant_seq=-;Dbxref=dbSNP_129:rs53578560;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	deletion	1175962	1175962	.	+	.	ID=5467;Variant_seq=-;Dbxref=dbSNP_129:rs53446407;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	deletion	1175967	1175967	.	+	.	ID=5468;Variant_seq=-;Dbxref=dbSNP_129:rs52955528;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1175969	1175969	.	+	.	ID=5469;Variant_seq=A;Dbxref=dbSNP_129:rs53001813;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1175983	1175983	.	+	.	ID=5470;Variant_seq=G;Dbxref=dbSNP_129:rs54385700;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1175999	1175999	.	+	.	ID=5471;Variant_seq=C;Dbxref=dbSNP_129:rs53268996;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1176003	1176003	.	+	.	ID=5472;Variant_seq=T;Dbxref=dbSNP_129:rs54357731;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1176042	1176042	.	+	.	ID=5473;Variant_seq=T;Dbxref=dbSNP_129:rs54181838;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1176088	1176088	.	+	.	ID=5474;Variant_seq=C;Dbxref=dbSNP_129:rs53997495;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1176091	1176091	.	+	.	ID=5475;Variant_seq=T;Dbxref=dbSNP_129:rs52926968;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	deletion	1176098	1176101	.	+	.	ID=5476;Variant_seq=-;Dbxref=dbSNP_129:rs53033778;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=TATA
5	dbSNP	SNV	1179204	1179204	.	+	.	ID=5477;Variant_seq=A;Dbxref=dbSNP_129:rs18061477;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1186613	1186613	.	+	.	ID=5478;Variant_seq=T;Dbxref=dbSNP_129:rs54126787;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1186689	1186689	.	+	.	ID=5479;Variant_seq=C;Dbxref=dbSNP_129:rs18750373;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1186699	1186699	.	+	.	ID=5480;Variant_seq=T;Dbxref=dbSNP_129:rs54308871;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1186700	1186700	.	+	.	ID=5481;Variant_seq=A;Dbxref=dbSNP_129:rs53296410;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1204720	1204720	.	+	.	ID=5482;Variant_seq=G;Dbxref=dbSNP_129:rs53747525;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1204739	1204739	.	+	.	ID=5483;Variant_seq=T;Dbxref=dbSNP_129:rs53846506;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1215911	1215911	.	+	.	ID=5484;Variant_seq=C;Dbxref=dbSNP_129:rs21272433;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1230028	1230028	.	+	.	ID=5485;Variant_seq=G;Dbxref=dbSNP_129:rs19032963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1230347	1230347	.	+	.	ID=5486;Variant_seq=T;Dbxref=dbSNP_129:rs19033083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1231844	1231844	.	+	.	ID=5487;Variant_seq=T;Dbxref=dbSNP_129:rs19033223;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1231941	1231941	.	+	.	ID=5488;Variant_seq=G;Dbxref=dbSNP_129:rs19033233;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1232495	1232495	.	+	.	ID=5489;Variant_seq=G;Dbxref=dbSNP_129:rs19035614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1233195	1233195	.	+	.	ID=5490;Variant_seq=A;Dbxref=dbSNP_129:rs53472270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1233250	1233250	.	+	.	ID=5491;Variant_seq=T;Dbxref=dbSNP_129:rs53130712;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	1233319	1233319	.	+	.	ID=5492;Variant_seq=ATAT;Dbxref=dbSNP_129:rs53572565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	1233618	1233618	.	+	.	ID=5493;Variant_seq=C;Dbxref=dbSNP_129:rs19033253;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1233620	1233620	.	+	.	ID=5494;Variant_seq=C;Dbxref=dbSNP_129:rs54007599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1233631	1233631	.	+	.	ID=5495;Variant_seq=G;Dbxref=dbSNP_129:rs19033263;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1234264	1234264	.	+	.	ID=5496;Variant_seq=C;Dbxref=dbSNP_129:rs19035754;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1234276	1234276	.	+	.	ID=5497;Variant_seq=C;Dbxref=dbSNP_129:rs19035764;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1234354	1234354	.	+	.	ID=5498;Variant_seq=C;Dbxref=dbSNP_129:rs19035774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1234435	1234435	.	+	.	ID=5499;Variant_seq=T;Dbxref=dbSNP_129:rs19035784;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1234826	1234826	.	+	.	ID=5500;Variant_seq=A;Dbxref=dbSNP_129:rs19035804;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1235135	1235135	.	+	.	ID=5501;Variant_seq=T;Dbxref=dbSNP_129:rs19035824;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1270868	1270868	.	+	.	ID=5502;Variant_seq=C;Dbxref=dbSNP_129:rs19032963;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1271188	1271188	.	+	.	ID=5503;Variant_seq=T;Dbxref=dbSNP_129:rs19033083;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1271809	1271809	.	+	.	ID=5504;Variant_seq=T;Dbxref=dbSNP_129:rs19033223;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1271906	1271906	.	+	.	ID=5505;Variant_seq=G;Dbxref=dbSNP_129:rs19033233;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1272465	1272465	.	+	.	ID=5506;Variant_seq=A;Dbxref=dbSNP_129:rs19035614;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1273166	1273166	.	+	.	ID=5507;Variant_seq=A;Dbxref=dbSNP_129:rs53472270;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1273221	1273221	.	+	.	ID=5508;Variant_seq=T;Dbxref=dbSNP_129:rs53130712;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	insertion	1273290	1273290	.	+	.	ID=5509;Variant_seq=ATAT;Dbxref=dbSNP_129:rs53572565;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=-
5	dbSNP	SNV	1273588	1273588	.	+	.	ID=5510;Variant_seq=C;Dbxref=dbSNP_129:rs19033253;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1273590	1273590	.	+	.	ID=5511;Variant_seq=C;Dbxref=dbSNP_129:rs54007599;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1273601	1273601	.	+	.	ID=5512;Variant_seq=G;Dbxref=dbSNP_129:rs19033263;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1274234	1274234	.	+	.	ID=5513;Variant_seq=C;Dbxref=dbSNP_129:rs19035754;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1274246	1274246	.	+	.	ID=5514;Variant_seq=C;Dbxref=dbSNP_129:rs19035764;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1274324	1274324	.	+	.	ID=5515;Variant_seq=C;Dbxref=dbSNP_129:rs19035774;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1274405	1274405	.	+	.	ID=5516;Variant_seq=T;Dbxref=dbSNP_129:rs19035784;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1274796	1274796	.	+	.	ID=5517;Variant_seq=A;Dbxref=dbSNP_129:rs19035804;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1275105	1275105	.	+	.	ID=5518;Variant_seq=T;Dbxref=dbSNP_129:rs19035824;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1276078	1276078	.	+	.	ID=5519;Variant_seq=G;Dbxref=dbSNP_129:rs19035855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1276345	1276345	.	+	.	ID=5520;Variant_seq=A;Dbxref=dbSNP_129:rs19035885;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1276358	1276358	.	+	.	ID=5521;Variant_seq=C;Dbxref=dbSNP_129:rs19035895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1276401	1276401	.	+	.	ID=5522;Variant_seq=A;Dbxref=dbSNP_129:rs19035905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1276434	1276434	.	+	.	ID=5523;Variant_seq=T;Dbxref=dbSNP_129:rs19035915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1276475	1276475	.	+	.	ID=5524;Variant_seq=T;Dbxref=dbSNP_129:rs19036375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1276489	1276489	.	+	.	ID=5525;Variant_seq=C;Dbxref=dbSNP_129:rs19036385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1276791	1276791	.	+	.	ID=5526;Variant_seq=A;Dbxref=dbSNP_129:rs19036395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1276826	1276826	.	+	.	ID=5527;Variant_seq=T;Dbxref=dbSNP_129:rs19036405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1276956	1276956	.	+	.	ID=5528;Variant_seq=T;Dbxref=dbSNP_129:rs19036415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1277208	1277208	.	+	.	ID=5529;Variant_seq=A;Dbxref=dbSNP_129:rs19036425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1299120	1299120	.	+	.	ID=5530;Variant_seq=T;Dbxref=dbSNP_129:rs19039591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1299280	1299280	.	+	.	ID=5531;Variant_seq=A;Dbxref=dbSNP_129:rs19039601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1310559	1310559	.	+	.	ID=5532;Variant_seq=A;Dbxref=dbSNP_129:rs19038250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1314216	1314216	.	+	.	ID=5533;Variant_seq=T;Dbxref=dbSNP_129:rs20446987;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1314634	1314634	.	+	.	ID=5534;Variant_seq=G;Dbxref=dbSNP_129:rs19036295;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1314787	1314787	.	+	.	ID=5535;Variant_seq=G;Dbxref=dbSNP_129:rs19036305;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1315941	1315941	.	+	.	ID=5536;Variant_seq=T;Dbxref=dbSNP_129:rs20446827;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1315980	1315980	.	+	.	ID=5537;Variant_seq=A;Dbxref=dbSNP_129:rs20446817;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1316849	1316849	.	+	.	ID=5538;Variant_seq=C;Dbxref=dbSNP_129:rs20446727;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1316889	1316889	.	+	.	ID=5539;Variant_seq=A;Dbxref=dbSNP_129:rs20446717;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1316889	1316889	.	+	.	ID=5540;Variant_seq=A;Dbxref=dbSNP_129:rs54054244;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1318951	1318951	.	+	.	ID=5541;Variant_seq=G;Dbxref=dbSNP_129:rs20446488;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1327061	1327061	.	+	.	ID=5542;Variant_seq=A;Dbxref=dbSNP_129:rs20445648;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1327427	1327427	.	+	.	ID=5543;Variant_seq=A;Dbxref=dbSNP_129:rs20445618;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1329885	1329885	.	+	.	ID=5544;Variant_seq=G;Dbxref=dbSNP_129:rs20443737;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1341300	1341300	.	+	.	ID=5545;Variant_seq=A;Dbxref=dbSNP_129:rs19035855;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1341567	1341567	.	+	.	ID=5546;Variant_seq=A;Dbxref=dbSNP_129:rs19035885;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1341580	1341580	.	+	.	ID=5547;Variant_seq=C;Dbxref=dbSNP_129:rs19035895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1341623	1341623	.	+	.	ID=5548;Variant_seq=A;Dbxref=dbSNP_129:rs19035905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1341656	1341656	.	+	.	ID=5549;Variant_seq=T;Dbxref=dbSNP_129:rs19035915;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1341697	1341697	.	+	.	ID=5550;Variant_seq=T;Dbxref=dbSNP_129:rs19036375;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1341711	1341711	.	+	.	ID=5551;Variant_seq=C;Dbxref=dbSNP_129:rs19036385;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1342013	1342013	.	+	.	ID=5552;Variant_seq=A;Dbxref=dbSNP_129:rs19036395;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1342048	1342048	.	+	.	ID=5553;Variant_seq=T;Dbxref=dbSNP_129:rs19036405;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1342178	1342178	.	+	.	ID=5554;Variant_seq=T;Dbxref=dbSNP_129:rs19036415;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1342430	1342430	.	+	.	ID=5555;Variant_seq=A;Dbxref=dbSNP_129:rs19036425;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1361289	1361289	.	+	.	ID=5556;Variant_seq=T;Dbxref=dbSNP_129:rs19038250;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1364962	1364962	.	+	.	ID=5557;Variant_seq=C;Dbxref=dbSNP_129:rs19038419;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1395322	1395322	.	+	.	ID=5558;Variant_seq=C;Dbxref=dbSNP_129:rs21752483;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1396747	1396747	.	+	.	ID=5559;Variant_seq=T;Dbxref=dbSNP_129:rs21602578;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1396784	1396784	.	+	.	ID=5560;Variant_seq=T;Dbxref=dbSNP_129:rs21368197;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1396823	1396823	.	+	.	ID=5561;Variant_seq=T;Dbxref=dbSNP_129:rs21602569;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1405202	1405202	.	+	.	ID=5562;Variant_seq=T;Dbxref=dbSNP_129:rs53930184;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1409120	1409120	.	+	.	ID=5563;Variant_seq=C;Dbxref=dbSNP_129:rs19039591;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1409280	1409280	.	+	.	ID=5564;Variant_seq=C;Dbxref=dbSNP_129:rs19039601;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1422908	1422908	.	+	.	ID=5565;Variant_seq=A;Dbxref=dbSNP_129:rs19090978;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1423085	1423085	.	+	.	ID=5566;Variant_seq=T;Dbxref=dbSNP_129:rs19039929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1424235	1424235	.	+	.	ID=5567;Variant_seq=A;Dbxref=dbSNP_129:rs19039929;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1424709	1424709	.	+	.	ID=5568;Variant_seq=A;Dbxref=dbSNP_129:rs19040145;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1439762	1439762	.	+	.	ID=5569;Variant_seq=A;Dbxref=dbSNP_129:rs21113740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1440790	1440790	.	+	.	ID=5570;Variant_seq=G;Dbxref=dbSNP_129:rs53045260;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1442725	1442725	.	+	.	ID=5571;Variant_seq=T;Dbxref=dbSNP_129:rs19041745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1442885	1442885	.	+	.	ID=5572;Variant_seq=A;Dbxref=dbSNP_129:rs19041755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1443746	1443746	.	+	.	ID=5573;Variant_seq=A;Dbxref=dbSNP_129:rs19041895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1443806	1443806	.	+	.	ID=5574;Variant_seq=A;Dbxref=dbSNP_129:rs19041905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1443868	1443868	.	+	.	ID=5575;Variant_seq=T;Dbxref=dbSNP_129:rs19041924;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1443938	1443938	.	+	.	ID=5576;Variant_seq=T;Dbxref=dbSNP_129:rs19041954;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1444501	1444501	.	+	.	ID=5577;Variant_seq=A;Dbxref=dbSNP_129:rs19042331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1444773	1444773	.	+	.	ID=5578;Variant_seq=G;Dbxref=dbSNP_129:rs19042341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1445220	1445220	.	+	.	ID=5579;Variant_seq=T;Dbxref=dbSNP_129:rs19042361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1445221	1445221	.	+	.	ID=5580;Variant_seq=T;Dbxref=dbSNP_129:rs19042371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1445361	1445361	.	+	.	ID=5581;Variant_seq=G;Dbxref=dbSNP_129:rs19042381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1448800	1448800	.	+	.	ID=5582;Variant_seq=C;Dbxref=dbSNP_129:rs52852972;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1448820	1448820	.	+	.	ID=5583;Variant_seq=A;Dbxref=dbSNP_129:rs18288634;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1449193	1449193	.	+	.	ID=5584;Variant_seq=C;Dbxref=dbSNP_129:rs19041745;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1449353	1449353	.	+	.	ID=5585;Variant_seq=G;Dbxref=dbSNP_129:rs19041755;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1451437	1451437	.	+	.	ID=5586;Variant_seq=A;Dbxref=dbSNP_129:rs19041895;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1451497	1451497	.	+	.	ID=5587;Variant_seq=C;Dbxref=dbSNP_129:rs19041905;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1451559	1451559	.	+	.	ID=5588;Variant_seq=C;Dbxref=dbSNP_129:rs19041924;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1451629	1451629	.	+	.	ID=5589;Variant_seq=C;Dbxref=dbSNP_129:rs19041954;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1462859	1462859	.	+	.	ID=5590;Variant_seq=T;Dbxref=dbSNP_129:rs19042221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1463648	1463648	.	+	.	ID=5591;Variant_seq=A;Dbxref=dbSNP_129:rs19042211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1472018	1472018	.	+	.	ID=5592;Variant_seq=G;Dbxref=dbSNP_129:rs20362522;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1475163	1475163	.	+	.	ID=5593;Variant_seq=A;Dbxref=dbSNP_129:rs19042570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1476095	1476095	.	+	.	ID=5594;Variant_seq=A;Dbxref=dbSNP_129:rs19042211;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1476884	1476884	.	+	.	ID=5595;Variant_seq=T;Dbxref=dbSNP_129:rs19042221;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1482077	1482077	.	+	.	ID=5596;Variant_seq=T;Dbxref=dbSNP_129:rs53154097;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1482427	1482427	.	+	.	ID=5597;Variant_seq=C;Dbxref=dbSNP_129:rs53939656;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1482841	1482841	.	+	.	ID=5598;Variant_seq=A;Dbxref=dbSNP_129:rs18921826;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1489023	1489023	.	+	.	ID=5599;Variant_seq=A;Dbxref=dbSNP_129:rs19042331;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1489295	1489295	.	+	.	ID=5600;Variant_seq=G;Dbxref=dbSNP_129:rs19042341;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1489743	1489743	.	+	.	ID=5601;Variant_seq=T;Dbxref=dbSNP_129:rs19042361;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1489744	1489744	.	+	.	ID=5602;Variant_seq=T;Dbxref=dbSNP_129:rs19042371;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1489884	1489884	.	+	.	ID=5603;Variant_seq=G;Dbxref=dbSNP_129:rs19042381;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1498919	1498919	.	+	.	ID=5604;Variant_seq=A;Dbxref=dbSNP_129:rs19042570;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1501393	1501393	.	+	.	ID=5605;Variant_seq=C;Dbxref=dbSNP_129:rs53790128;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1501919	1501919	.	+	.	ID=5606;Variant_seq=A;Dbxref=dbSNP_129:rs19042710;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1502564	1502564	.	+	.	ID=5607;Variant_seq=C;Dbxref=dbSNP_129:rs19042730;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1503284	1503284	.	+	.	ID=5608;Variant_seq=C;Dbxref=dbSNP_129:rs19042740;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1503766	1503766	.	+	.	ID=5609;Variant_seq=G;Dbxref=dbSNP_129:rs19042750;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1503945	1503945	.	+	.	ID=5610;Variant_seq=G;Dbxref=dbSNP_129:rs19042760;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1505068	1505068	.	+	.	ID=5611;Variant_seq=G;Dbxref=dbSNP_129:rs19042770;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1505473	1505473	.	+	.	ID=5612;Variant_seq=C;Dbxref=dbSNP_129:rs19042780;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1505928	1505928	.	+	.	ID=5613;Variant_seq=A;Dbxref=dbSNP_129:rs19042800;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1505937	1505937	.	+	.	ID=5614;Variant_seq=T;Dbxref=dbSNP_129:rs19042810;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1507678	1507678	.	+	.	ID=5615;Variant_seq=T;Dbxref=dbSNP_129:rs21697368;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1533803	1533803	.	+	.	ID=5616;Variant_seq=A;Dbxref=dbSNP_129:rs19078314;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1533911	1533911	.	+	.	ID=5617;Variant_seq=T;Dbxref=dbSNP_129:rs19078324;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1533995	1533995	.	+	.	ID=5618;Variant_seq=G;Dbxref=dbSNP_129:rs19078354;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1534025	1534025	.	+	.	ID=5619;Variant_seq=G;Dbxref=dbSNP_129:rs19078364;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1534034	1534034	.	+	.	ID=5620;Variant_seq=G;Dbxref=dbSNP_129:rs19078374;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1534060	1534060	.	+	.	ID=5621;Variant_seq=T;Dbxref=dbSNP_129:rs19078384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1534179	1534179	.	+	.	ID=5622;Variant_seq=T;Dbxref=dbSNP_129:rs19078394;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1534213	1534213	.	+	.	ID=5623;Variant_seq=T;Dbxref=dbSNP_129:rs53957392;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1534222	1534222	.	+	.	ID=5624;Variant_seq=C;Dbxref=dbSNP_129:rs53219434;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1534224	1534224	.	+	.	ID=5625;Variant_seq=A;Dbxref=dbSNP_129:rs53813384;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1534241	1534241	.	+	.	ID=5626;Variant_seq=T;Dbxref=dbSNP_129:rs19078404;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1534244	1534244	.	+	.	ID=5627;Variant_seq=T;Dbxref=dbSNP_129:rs54386149;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=A
5	dbSNP	SNV	1534259	1534259	.	+	.	ID=5628;Variant_seq=A;Dbxref=dbSNP_129:rs54280487;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1534260	1534260	.	+	.	ID=5629;Variant_seq=C;Dbxref=dbSNP_129:rs53639758;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1534278	1534278	.	+	.	ID=5630;Variant_seq=A;Dbxref=dbSNP_129:rs53726047;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1534283	1534283	.	+	.	ID=5631;Variant_seq=C;Dbxref=dbSNP_129:rs53351057;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1534289	1534289	.	+	.	ID=5632;Variant_seq=T;Dbxref=dbSNP_129:rs54060373;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=C
5	dbSNP	SNV	1534291	1534291	.	+	.	ID=5633;Variant_seq=C;Dbxref=dbSNP_129:rs54083347;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1534320	1534320	.	+	.	ID=5634;Variant_seq=C;Dbxref=dbSNP_129:rs53445118;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=T
5	dbSNP	SNV	1534326	1534326	.	+	.	ID=5635;Variant_seq=A;Dbxref=dbSNP_129:rs54200545;ensembl_failure_reason=Variant maps to more than one genomic location;Reference_seq=G
5	dbSNP	SNV	1534338	1534338