chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43970492839704929AG43GENIChomozygous56840052
43970526039705261GA30GENIChomozygous56840053
43970556039705561CT25GENICpossibly homozygous56840054
43970562739705628AC16GENIChomozygous56840055
43970565139705652TG16GENIChomozygous56840056
43970590239705903CCT21GENIChomozygous56840057
43970590639705907A-20GENIChomozygous56840058
43970632139706322GA43GENIChomozygous56840059
43970636339706364T-2GENIChomozygous56840060
43970637639706377AG35GENIChomozygous56840061
43970652539706526AT20GENIChomozygous56840062
43970660739706608TC15GENIChomozygous56840063
43970671239706713GA31GENIChomozygous56840064
43970703239707033CT51GENICpossibly homozygous56840065
43970730539707306CT44GENIChomozygous56840066
43970740039707401CA32GENIChomozygous56840067
43970761139707612TC47GENICheterozygous56840068
43970767739707678CT45GENICpossibly homozygous56840069
43970773139707732AT49GENIChomozygous56840070
43970789539707896CG17GENIChomozygous56840071
43970790739707908AC19GENIChomozygous56840072
43970809539708096AG29GENIChomozygous56840073
43970833439708335CA22GENIChomozygous56840074
43970839239708393GA23GENICpossibly homozygous56840075
43970846539708466CT16GENICheterozygous56840076
43970862239708623TTGAA3GENIChomozygous56840077
43970910039709101TC129GENICheterozygous56840078
43970931039709311AG26GENICpossibly homozygous56840079
43970933839709339GA29GENIChomozygous56840080
43970949739709498TC18GENICheterozygous56840081
43970951539709516CA18GENICheterozygous56840082
43970951839709519GA15GENICheterozygous56840083
43970995139709952GA34GENICheterozygous56840084
43971065239710653GA19GENIChomozygous56840085
43971074639710747TC42GENICpossibly homozygous56840086
43971080239710803TA35GENIChomozygous56840087
43971108339711084TC30GENIChomozygous56840088
43971122539711226AG19GENIChomozygous56840089