chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182616362026163621CT61GENIChomozygous140291461
182616383326163834GC43GENIChomozygous140291462
182616383526163836AT43GENIChomozygous140291463
182616395626163957TG46GENIChomozygous140291464
182616398426163985CT50GENIChomozygous140291465
182616459026164590ACACACGG25GENIChomozygous140216934
182616535126165355AAAC37GENIChomozygous140216935
182616542326165424TG44GENIChomozygous140291466
182616570126165702TC49GENIChomozygous140291467
182616599026165991AG41GENIChomozygous140291468
182616599426165995TA42GENIChomozygous140291469
182616616926166170GT45GENIChomozygous140291470
182616634626166346AAG44GENIChomozygous140216936
182616752026167531AGCTGTTAATG30GENIChomozygous140216937
182616836426168365AG40GENIChomozygous140291471
182616904026169041T26GENICpossibly homozygous140216938
182616945726169458GA45GENIChomozygous140291472
182616958426169585TC47GENIChomozygous140291473
182617036626170367TC44GENIChomozygous140291474
182617146926171470G32GENIChomozygous140216939
182617147226171479AGGAAGG32GENIChomozygous140216940
182617147826171479G32GENIChomozygous403862130
182617147826171479GA32GENICheterozygous403862131
182617147426171475G32GENIChomozygous403862128
182617147426171475GA32GENICheterozygous403862129
182617164726171648AG7GENIChomozygous140291475
182617165526171656A7GENIChomozygous140216941
182617167226171672AAG6GENIChomozygous140216942
182617261126172612AT38GENIChomozygous140291476
182617308526173086AG42GENIChomozygous140291477
182617407826174079AT43GENIChomozygous140291478
182617509526175096GT16GENICpossibly homozygous140291479
182617588126175882TC29GENIChomozygous140291480
182617715126177152GA41GENIChomozygous140291481
182617750126177501T42GENIChomozygous140216943
182617799826177999GA36GENIChomozygous140291482