chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71177043311770434CT58GENIChomozygous780664549
71177196711771968TC23GENIChomozygous780664550
71177197011771971GA24GENICpossibly homozygous780664551
71177263311772634GA51GENICpossibly homozygous780664552
71177348211773483GA66GENIChomozygous780664553
71177377311773774GA46GENICpossibly homozygous780664554
71177412511774126AC44GENIChomozygous780664555
71177432011774321CT41GENIChomozygous780664556