chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148109205481092055AAT10GENICpossibly homozygous745033253
148109223381092234GA12GENIChomozygous629519899
148109320281093206TTTT----1GENIChomozygous745033254
148109373881093739A-1GENIChomozygous745033257
148109497481094975CT25GENIChomozygous629519900
148109524781095248T-17GENIChomozygous745033263
148109598381095984GA11GENICpossibly homozygous629519901
148109606081096061GA10GENICheterozygous629519902
148109623281096233TC14GENICpossibly homozygous629519903
148109654281096543CT8GENIChomozygous629519904
148109740781097408CT4GENIChomozygous629519905
148109809681098097AT11GENIChomozygous629519906
148109827381098274TTC2GENICheterozygous745033264
148109829081098291CT6GENICheterozygous629519907
148109925081099251CT5GENICheterozygous629519908