chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT9GENIChomozygous933234614
141761650017616501GA12GENIChomozygous933234615
141761696917616970TA3GENIChomozygous933234616
141761774217617743CA10GENICpossibly homozygous933234617
141761922817619229TA9GENIChomozygous933234618
141762090817620909GA4GENIChomozygous933234619
141762138217621383TC14GENIChomozygous933234620
141762151417621515CT13GENIChomozygous933234621
141762219917622200CT8GENIChomozygous933234622
141762256517622566TA20GENIChomozygous933234623
141762525917625260GA11GENIChomozygous933234624
141762542117625422AC10GENIChomozygous933234625
141762588517625886AG9GENIChomozygous933234626
141762752017627521CT10GENIChomozygous933234627
141762915917629160GT6GENIChomozygous933234628
141763031317630314GA3GENIChomozygous933234629
141763041317630414CG10GENIChomozygous933234630