chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5170248538170248539GA15GENICpossibly homozygous56087799
5170252217170252218AG14GENICpossibly homozygous56087802
5170254063170254064GC21GENIChomozygous56087803
5170254722170254723CCT7GENICheterozygous56087804
5170255257170255258AG24GENIChomozygous56087805
5170255966170255967AG7GENIChomozygous56087806
5170257128170257129AG16GENICpossibly homozygous56087807
5170257677170257678TC15GENIChomozygous56087808
5170258915170258916AG25GENICpossibly homozygous56087810
5170259553170259554C-15GENIChomozygous55838407
5170259643170259644GA9GENICpossibly homozygous56087811
5170260198170260199T-10GENICpossibly homozygous56087812
5170264871170264872GA19GENIChomozygous56087814
5170265104170265105GA22GENICpossibly homozygous56087815
5170269033170269034CT7GENIChomozygous56087816
5170270204170270205TA8GENICpossibly homozygous55838410
5170271755170271756TC8GENIChomozygous56087817
5170272315170272316AG9GENIChomozygous56087819
5170272196170272198AA--1GENIChomozygous56365073
5170260199170260200GC10GENICpossibly homozygous56365072