chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT18GENIChomozygous113578070
141761650017616501GA22GENIChomozygous113578071
141761696917616970TA20GENIChomozygous113578072
141761774217617743CA21GENIChomozygous113578073
141761922817619229TA28GENIChomozygous113578074
141762090817620909GA19GENIChomozygous113578075
141762138217621383TC35GENIChomozygous113362772
141762151417621515CT39GENIChomozygous113578076
141762219917622200CT30GENIChomozygous113578077
141762256517622566TA25GENIChomozygous113362774
141762525917625260GA34GENIChomozygous113578078
141762542117625422AC22GENICpossibly homozygous113578079
141762588517625886AG16GENIChomozygous113362781
141762752017627521CT18GENIChomozygous113578080
141762915917629160GT19GENIChomozygous113578081
141763031317630314GA27GENIChomozygous113578082
141763041317630414CG19GENIChomozygous113578083