chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43970492839704929AG21GENIChomozygous56840052
43970526039705261GA5GENIChomozygous56840053
43970556039705561CT17GENIChomozygous56840054
43970562739705628AC16GENIChomozygous56840055
43970565139705652TG17GENIChomozygous56840056
43970590239705903CCT12GENIChomozygous56840057
43970590639705907A-12GENIChomozygous56840058
43970632139706322GA22GENIChomozygous56840059
43970637639706377AG10GENIChomozygous56840061
43970652539706526AT7GENIChomozygous56840062
43970660739706608TC3GENIChomozygous56840063
43970671239706713GA24GENIChomozygous56840064
43970703239707033CT25GENICpossibly homozygous56840065
43970730539707306CT22GENIChomozygous56840066
43970740039707401CA43GENIChomozygous56840067
43970761139707612TC26GENICpossibly homozygous56840068
43970767739707678CT26GENICpossibly homozygous56840069
43970773139707732AT22GENIChomozygous56840070
43970789539707896CG18GENIChomozygous56840071
43970790739707908AC17GENIChomozygous56840072
43970809539708096AG18GENICpossibly homozygous56840073
43970833439708335CA16GENIChomozygous56840074
43970839239708393GA7GENIChomozygous56840075
43970846539708466CT13GENICheterozygous56840076
43970862239708623TTGAA1GENIChomozygous56840077
43970910039709101TC62GENICheterozygous56840078
43970931039709311AG12GENICpossibly homozygous56840079
43970933839709339GA14GENIChomozygous56840080
43970949739709498TC13GENICheterozygous56840081
43970995139709952GA31GENICheterozygous56840084
43971065239710653GA19GENIChomozygous56840085
43971074639710747TC15GENIChomozygous56840086
43971080239710803TA12GENIChomozygous56840087
43971108339711084TC14GENIChomozygous56840088
43971122539711226AG16GENIChomozygous56840089