chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170621280170621281GA18GENIChomozygous61960434
1170622513170622517ACAC----1GENIChomozygous62544948
1170622756170622757TC17GENIChomozygous60941111
1170623122170623123CA25GENIChomozygous60941112
1170623538170623539AG24GENIChomozygous61960435
1170623869170623870GA19GENIChomozygous61960436
1170624065170624066TC10GENIChomozygous61960437
1170624310170624311CA14GENIChomozygous61960438
1170624640170624641CT8GENIChomozygous61960439
1170624805170624806CT18GENIChomozygous61960440
1170625066170625067CA9GENIChomozygous61960442
1170625107170625108GA22GENIChomozygous61960443
1170624336170624337TTCACACACACACA5GENIChomozygous62173309
1170626767170626771ACAC----1GENIChomozygous62173311
1170627910170627911GC2GENIChomozygous61960444
1170628709170628710AG23GENIChomozygous60941115
1170629075170629076GGAA8GENICheterozygous60941116
1170629076170629077A-8GENICheterozygous61909305
1170629637170629638GA13GENICpossibly homozygous60941117
1170631445170631446TC19GENIChomozygous60941118
1170631481170631482C-15GENIChomozygous60941120
1170631487170631488AC17GENIChomozygous62173313
1170632111170632112CT25GENIChomozygous61960446
1170632202170632203TC15GENIChomozygous60941121