chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182503996625039967TA55GENIChomozygous110309751
182504124725041248AG34GENIChomozygous110309753
182504144725041448GA24GENIChomozygous110309755
182504244325042444CT25GENIChomozygous110309757
182504323825043239TC27GENIChomozygous110309759
182504480625044807TG36GENIChomozygous110309761
182504621125046212GA19GENIChomozygous110309763
182504623125046232CT21GENIChomozygous110309765
182504772925047730AG24GENIChomozygous110309767
182504877925048780CT25GENIChomozygous110309769
182504888125048882TA25GENIChomozygous110309771
182504903925049040AG30GENIChomozygous110309773
182505077425050775TC34GENICpossibly homozygous110309775
182505279625052797CT27GENIChomozygous110309777
182505285225052853GA28GENIChomozygous110309778
182505355325053554TA21GENIChomozygous110309779
182505730925057310GA22GENIChomozygous110309780
182505793725057938CT30GENIChomozygous110309781
182506089825060899TC22GENIChomozygous110309782
182506372725063728CT34GENIChomozygous110309783
182506389025063891GA25GENIChomozygous110309784
182506407125064072GT20GENIChomozygous110309785
182506428125064282CA14GENIChomozygous110309786