chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176710672176710673GA58GENIChomozygous112219110
3176712180176712181GA70GENIChomozygous112219111
3176712217176712218TC60GENIChomozygous112219112
3176714300176714301CT48GENIChomozygous112219114
3176715430176715431CT67GENIChomozygous112219115
3176714376176714377TC52GENICpossibly homozygous119686725
3176713416176713420GGAG9GENICpossibly homozygous131333440