chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225151889225151890TC67GENICpossibly homozygous108556559
1225155073225155074AG50GENIChomozygous108556560
1225156307225156308CT76GENICpossibly homozygous108556561
1225157017225157018AT31GENIChomozygous108556562
1225157019225157020TC31GENIChomozygous108556563
1225157236225157237AG53GENICpossibly homozygous108556564
1225157833225157834GA65GENIChomozygous108556565
1225158527225158528GA64GENIChomozygous108556566