chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176710672176710673GA49GENICpossibly homozygous112219110
3176712180176712181GA62GENIChomozygous112219111
3176712217176712218TC58GENIChomozygous112219112
3176713416176713420GGAG13GENIChomozygous131333440
3176714300176714301CT49GENIChomozygous112219114
3176715430176715431CT61GENIChomozygous112219115
3176714376176714377TC47GENIChomozygous119686725