chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2270833533270833534GA11GENICpossibly homozygous59571702
2270834817270834818TG9GENICpossibly homozygous59571703
2270835779270835780CG17GENIChomozygous59571704
2270835977270835978CT17GENIChomozygous59571705
2270836723270836724CT13GENICheterozygous60264799
2270837921270837923AC--3GENICheterozygous59571709
2270839524270839525CT8GENIChomozygous59571712
2270840623270840624AG1GENIChomozygous59571713
2270843206270843207AG7GENIChomozygous59571715
2270844190270844191GA6GENIChomozygous59571716
2270846024270846028AAAG----4GENIChomozygous59571717
2270846144270846145CT17GENICpossibly homozygous59571718