chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96508739565087396CCG7GENIChomozygous52006794
96508740765087408GGC9GENIChomozygous52006795
96508740965087410CCAG9GENIChomozygous52006796
96508741265087413CCCT10GENIChomozygous52006797
96508847265088473TTG13GENICheterozygous52006802
96508847265088473TTGG13GENICheterozygous52006803
96508877165088772TC24GENIChomozygous52006807
96508895565088956CCTTTT12GENICheterozygous52006809
96508895565088956CCTTT12GENICheterozygous52227722
96508942465089425T-21GENIChomozygous52006811
96508943965089443TTTT----22GENIChomozygous52227723
96508945865089459T-18GENIChomozygous52227724
96508945965089460TG18GENIChomozygous52909563
96508948165089482AG19GENIChomozygous52227725
96508955665089557TC24GENICpossibly homozygous52006813
96508967665089677GA23GENIChomozygous52006815
96508977365089774CT27GENIChomozygous52227726
96508989465089895CT23GENIChomozygous52006817
96509053065090531GA22GENIChomozygous52006819
96509085665090857GC27GENIChomozygous52227727
96509218065092181GT16GENIChomozygous52855952
96509235365092355AG--19GENIChomozygous52227728
96509276465092765CT24GENIChomozygous52006837
96509284765092848AG30GENIChomozygous52227729
96509340865093409CT27GENIChomozygous52227730
96509381465093815TTAGCCC31GENIChomozygous52006842
96509381565093816TA31GENIChomozygous52855954
96509399465093995GT28GENIChomozygous52400443
96509442065094421GGA17GENICpossibly homozygous52227731
96509461965094620GA26GENIChomozygous52227732
96509555265095553AG30GENIChomozygous52227733
96509585565095856GC19GENIChomozygous52227734
96509606665096067GC19GENICpossibly homozygous52227735
96509665965096660GA26GENIChomozygous52227736
96509684265096843TC25GENIChomozygous52006847
96509792065097921AG23GENICpossibly homozygous52006851
96509798965097991GG--20GENIChomozygous52400445
96509922065099221TC30GENIChomozygous52006857
96509984065099841CT20GENIChomozygous52006858