chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT28GENIChomozygous809188123
141761650017616501GA31GENIChomozygous809188124
141761696917616970TA44GENIChomozygous809188125
141761774217617743CA46GENIChomozygous809188126
141761922817619229TA45GENIChomozygous809188127
141761998817619989GA45GENICpossibly homozygous809188128
141762090817620909GA38GENICpossibly homozygous809188129
141762138217621383TC40GENIChomozygous809188130
141762151417621515CT51GENIChomozygous809188131
141762219917622200CT67GENICpossibly homozygous809188132
141762256517622566TA53GENICpossibly homozygous809188133
141762525917625260GA46GENIChomozygous809188134
141762542117625422AC45GENIChomozygous809188135
141762588517625886AG53GENICpossibly homozygous809188136
141762752017627521CT24GENIChomozygous809188137
141762915917629160GT48GENIChomozygous809188138
141763031317630314GA55GENIChomozygous809188139
141763041317630414CG51GENIChomozygous809188140