chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175442686175442687GC8GENICheterozygous403127987
4175442686175442687G8GENICpossibly homozygous403127988
4175442688175442689GC8GENICheterozygous403127989
4175442688175442689G8GENICpossibly homozygous403127990
4175444827175444828TG17GENIChomozygous141674645
4175444994175444995TC14GENIChomozygous141674646