chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101860184101860185AG31GENICpossibly homozygous51585819
10101860190101860191AG31GENICpossibly homozygous51585821
10101860625101860626AATT9GENIChomozygous51585823
10101861251101861252TC61GENICheterozygous51585825
10101872114101872115AG15GENIChomozygous51585827
10101872530101872542GAGAGAGAGAGA------------9GENIChomozygous51585829
10101875230101875231AAT20GENIChomozygous51585831
10101876421101876422G-7GENICheterozygous51585833
10101872553101872554AC18GENICheterozygous51998841