chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT26GENIChomozygous804589091
141761650017616501GA15GENIChomozygous804589092
141761696917616970TA11GENIChomozygous804589093
141761774217617743CA18GENIChomozygous804589094
141761922817619229TA12GENIChomozygous804589095
141761998817619989GA33GENICpossibly homozygous804589096
141762090817620909GA16GENIChomozygous804589097
141762138217621383TC13GENIChomozygous804589098
141762151417621515CT12GENIChomozygous804589099
141762219917622200CT30GENIChomozygous804589100
141762256517622566TA28GENICpossibly homozygous804589101
141762525917625260GA18GENIChomozygous804589102
141762542117625422AC20GENIChomozygous804589103
141762588517625886AG16GENIChomozygous804589104
141762752017627521CT26GENIChomozygous804589105
141762915917629160GT17GENIChomozygous804589106
141763031317630314GA20GENIChomozygous804589107
141763041317630414CG24GENIChomozygous804589108