chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761847117618472TA22GENIChomozygous976955533
141762138217621383TC36GENIChomozygous976955534
141762256517622566TA33GENIChomozygous976955535
141762305917623060TC12GENIChomozygous976955536
141762436417624365CT24GENIChomozygous976955537
141762439017624391TC28GENIChomozygous976955538
141762549717625498AC19GENICheterozygous976955539
141762588517625886AG20GENIChomozygous976955540
141762709017627091CA33GENIChomozygous976955541
141762915917629160GT11GENIChomozygous976955542
141762980417629805AG28GENIChomozygous976955543
141762980517629806CA27GENIChomozygous976955544
141762981017629811AG27GENIChomozygous976955545
141763140917631410CT26GENIChomozygous976955546