chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761607817616079AG24GENICheterozygous980250571
141761639017616391CT30GENIChomozygous980250572
141761847117618472TA32GENIChomozygous980250573
141762138217621383TC47GENIChomozygous980250574
141762256517622566TA26GENIChomozygous980250575
141762305917623060TC37GENIChomozygous980250576
141762436417624365CT37GENIChomozygous980250577
141762439017624391TC43GENIChomozygous980250578
141762588517625886AG19GENIChomozygous980250579
141762709017627091CA40GENIChomozygous980250580
141762915917629160GT25GENIChomozygous980250581
141762980417629805AG18GENIChomozygous980250582
141762980517629806CA17GENIChomozygous980250583
141762981017629811AG19GENIChomozygous980250584
141763140917631410CT35GENIChomozygous980250585