chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1123098312123098313AG51GENIChomozygous108210890
1123098878123098879CG61GENICpossibly homozygous108210891
1123099106123099107GA56GENIChomozygous108210892
1123099206123099207TG52GENIChomozygous108210893
1123099322123099323CT47GENIChomozygous108210894
1123099445123099446CT58GENICpossibly homozygous108210895
1123100115123100116CG41GENIChomozygous108210896