chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT16GENIChomozygous959117749
141761650017616501GA12GENICpossibly homozygous959117750
141761696917616970TA18GENIChomozygous959117751
141761774217617743CA21GENIChomozygous959117752
141761922817619229TA28GENIChomozygous959117753
141761998817619989GA22GENIChomozygous959117754
141762090817620909GA17GENIChomozygous959117755
141762138217621383TC31GENIChomozygous959117756
141762151417621515CT21GENIChomozygous959117757
141762219917622200CT31GENIChomozygous959117758
141762256517622566TA18GENIChomozygous959117759
141762525917625260GA17GENIChomozygous959117760
141762542117625422AC7GENIChomozygous959117761
141762588517625886AG17GENIChomozygous959117762
141762752017627521CT9GENIChomozygous959117763
141762915917629160GT27GENIChomozygous959117764
141763031317630314GA20GENIChomozygous959117765
141763041317630414CG22GENIChomozygous959117766