chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71177043311770434CT50GENIChomozygous775760960
71177196711771968TC35GENICpossibly homozygous775760961
71177197011771971GA33GENIChomozygous775760962
71177263311772634GA23GENIChomozygous775760963
71177348211773483GA33GENIChomozygous775760964
71177377311773774GA34GENIChomozygous775760965
71177412511774126AC42GENIChomozygous775760966
71177432011774321CT42GENIChomozygous775760967