chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53589351535893515A56GENICpossibly homozygous128168974
53589574635895747TC43GENIChomozygous113742096
53589623135896232AG50GENIChomozygous113742098
53589723335897236ATA47GENIChomozygous128168975
53589805435898055A45GENIChomozygous128168976
53589810935898110AG58GENIChomozygous113742100
53589908635899087CA57GENIChomozygous113742102
53589963635899636TAT42GENIChomozygous128168977
53590000435900005A45GENIChomozygous128168978
53590010235900102TTTCTGCCAAGA43GENIChomozygous128168979
53590052935900530TC55GENIChomozygous113742104
53590096235900963GT40GENIChomozygous113742106