chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96508732165087322AAG9GENIChomozygous52227721
96508739565087396CCG7GENIChomozygous52006794
96508740765087408GGC7GENIChomozygous52006795
96508740965087410CCAG4GENIChomozygous52006796
96508741265087413CCCT6GENIChomozygous52006797
96508847265088473TTG13GENICheterozygous52006802
96508847265088473TTGG13GENICpossibly homozygous52006803
96508877165088772TC23GENIChomozygous52006807
96508895565088956CCTTTT5GENICheterozygous52006809
96508895565088956CCTTT5GENICheterozygous52227722
96508942465089425T-11GENIChomozygous52006811
96508943965089443TTTT----14GENICpossibly homozygous52227723
96508945865089459T-6GENIChomozygous52227724
96508948165089482AG8GENIChomozygous52227725
96508955665089557TC19GENIChomozygous52006813
96508967665089677GA25GENIChomozygous52006815
96508977365089774CT29GENIChomozygous52227726
96508989465089895CT29GENIChomozygous52006817
96509053065090531GA26GENIChomozygous52006819
96509085665090857GC25GENIChomozygous52227727
96509235365092355AG--20GENIChomozygous52227728
96509276465092765CT19GENIChomozygous52006837
96509284765092848AG20GENIChomozygous52227729
96509340865093409CT37GENIChomozygous52227730
96509381465093815TTAGCCC15GENIChomozygous52006842
96509442065094421GGA13GENIChomozygous52227731
96509461965094620GA26GENIChomozygous52227732
96509555265095553AG37GENICpossibly homozygous52227733
96509585565095856GC16GENIChomozygous52227734
96509606665096067GC20GENIChomozygous52227735
96509665965096660GA17GENIChomozygous52227736
96509684265096843TC27GENIChomozygous52006847
96509792065097921AG35GENICpossibly homozygous52006851
96509799065097991G-21GENICpossibly homozygous52006852
96509922065099221TC17GENIChomozygous52006857
96509984065099841CT9GENIChomozygous52006858
96509399465093995GT18GENIChomozygous52400443
96509798965097991GG--21GENICheterozygous52400445