chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X24817582481759AC5GENIChomozygous45076774
X24845782484579GT15GENIChomozygous45076775
X24854802485481AG17GENIChomozygous45076776
X24865112486512AG3GENIChomozygous45076777
X24898582489859TA7GENIChomozygous45076778
X24903982490399TTTA8GENIChomozygous45076779
X24909242490925GGAC7GENICpossibly homozygous45076780
X24924692492470AG2GENIChomozygous45076781
X24947152494716TA10GENIChomozygous45076782
X24965912496592AG8GENIChomozygous45076783
X24971362497137AG10GENIChomozygous45076784