chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1220697042069705CT10GENIChomozygous126162459
1220700422070043AG21GENIChomozygous126162460
1220716452071646CG24GENIChomozygous126162462
1220716982071699CT16GENIChomozygous126162463
1220718982071899AG11GENIChomozygous126162464
1220721152072116AG11GENIChomozygous126162465
1220722622072263AG8GENIChomozygous126208216
1220724282072429GT8GENIChomozygous126162466
1220724452072446GT5GENIChomozygous126162467
1220725352072536GT15GENIChomozygous126162468
1220728972072898AC15GENIChomozygous126162469
1220733552073356CG16GENIChomozygous126162470
1220736622073663GT15GENICheterozygous126162471
1220737372073738AG21GENIChomozygous126162472
1220737952073796AG15GENIChomozygous126162473
1220751262075127CA19GENIChomozygous126162474
1220752622075263CT8GENIChomozygous126162475
1220774552077456AT14GENIChomozygous126162476
1220798852079886AG4GENIChomozygous126222796
1220850772085078TA9GENIChomozygous126162477
1220897892089790TC6GENIChomozygous126162478
1220933712093372GA13GENIChomozygous126162479
1220968942096895CT10GENIChomozygous126162481