chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182503996625039967TA19GENIChomozygous110309751
182504124725041248AG23GENIChomozygous110309753
182504144725041448GA23GENIChomozygous110309755
182504244325042444CT16GENIChomozygous110309757
182504323825043239TC22GENIChomozygous110309759
182504480625044807TG16GENIChomozygous110309761
182504621125046212GA13GENIChomozygous110309763
182504623125046232CT21GENIChomozygous110309765
182504772925047730AG20GENIChomozygous110309767
182504877925048780CT12GENIChomozygous110309769
182504903925049040AG16GENIChomozygous110309773
182505077425050775TC13GENIChomozygous110309775
182505279625052797CT20GENIChomozygous110309777
182505285225052853GA6GENIChomozygous110309778
182505355325053554TA12GENIChomozygous110309779
182505730925057310GA21GENIChomozygous110309780
182505774625057747GA9GENIChomozygous110647645
182505793725057938CT24GENIChomozygous110309781
182506001125060012TA9GENICheterozygous119485445
182506089825060899TC17GENIChomozygous110309782
182506372725063728CT10GENIChomozygous110309783
182506389025063891GA17GENIChomozygous110309784
182506428125064282CA16GENIChomozygous110309786