chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118095439118095440TTG20GENIChomozygous54079143
7118095552118095553TC30GENIChomozygous54231632
7118096969118096970TC36GENIChomozygous54231634
7118097732118097733TC24GENIChomozygous54231636
7118098117118098118GC32GENIChomozygous54231638
7118098457118098458TC27GENIChomozygous54231640
7118099315118099316AT27GENIChomozygous54231642
7118099951118099952A-8GENIChomozygous55000624
7118101016118101017TTC13GENICpossibly homozygous54231646
7118101187118101188AG22GENIChomozygous54079144
7118101370118101371CT12GENIChomozygous54231648
7118101419118101420CT17GENIChomozygous54231650
7118101560118101561CT22GENIChomozygous54231652