chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71177043311770434CT26GENIChomozygous961255807
71177263311772634GA17GENIChomozygous961255808
71177348211773483GA12GENIChomozygous961255809
71177377311773774GA11GENIChomozygous961255810
71177412511774126AC17GENIChomozygous961255811
71177432011774321CT30GENICpossibly homozygous961255812