chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT34GENIChomozygous795637313
141761650017616501GA31GENIChomozygous795637314
141761696917616970TA58GENIChomozygous795637315
141761774217617743CA51GENICpossibly homozygous795637316
141761922817619229TA56GENIChomozygous795637317
141761998817619989GA44GENIChomozygous795637318
141762090817620909GA27GENIChomozygous795637319
141762138217621383TC36GENIChomozygous795637320
141762151417621515CT32GENIChomozygous795637321
141762219917622200CT22GENIChomozygous795637322
141762256517622566TA46GENIChomozygous795637323
141762525917625260GA39GENIChomozygous795637324
141762542117625422AC40GENIChomozygous795637325
141762588517625886AG57GENIChomozygous795637326
141762752017627521CT41GENIChomozygous795637327
141762915917629160GT28GENIChomozygous795637328
141763031317630314GA39GENIChomozygous795637329
141763041317630414CG55GENIChomozygous795637330