chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118095439118095440TTG15GENIChomozygous54079143
7118095552118095553TC14GENIChomozygous54231632
7118096969118096970TC15GENIChomozygous54231634
7118097732118097733TC10GENIChomozygous54231636
7118098117118098118GC14GENIChomozygous54231638
7118098457118098458TC17GENIChomozygous54231640
7118099315118099316AT29GENIChomozygous54231642
7118099951118099952A-6GENIChomozygous55000624
7118101016118101017TTC9GENIChomozygous54231646
7118101187118101188AG16GENIChomozygous54079144
7118101370118101371CT9GENIChomozygous54231648
7118101419118101420CT12GENIChomozygous54231650
7118101560118101561CT5GENIChomozygous54231652