chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74097937740979378AG12GENICpossibly homozygous53888771
74097954940979550TC13GENIChomozygous53888772
74098062740980628GT13GENIChomozygous54364887
74098067340980674TA8GENIChomozygous54364889
74098102540981026GGC19GENICpossibly homozygous53888774
74098156240981563GA15GENIChomozygous54364891
74098160040981601TC13GENICheterozygous53888775
74098174840981749GA15GENIChomozygous54364893
74098199140981992CT22GENIChomozygous54364895
74098271840982719GT18GENIChomozygous54364897