chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134773940047739401AC16GENIChomozygous49751928
134773962347739624TC20GENICpossibly homozygous49751929
134773965547739656TC21GENIChomozygous49751930
134774008847740089CT24GENIChomozygous49751931
134774031347740314GA17GENIChomozygous49751932
134774035847740359AG16GENIChomozygous49751933
134774037447740375AG15GENIChomozygous49751934
134774037647740377GA16GENIChomozygous49751935
134774052647740527TC17GENIChomozygous49751936
134774052947740530AC15GENIChomozygous49751937
134774078747740788AG21GENIChomozygous49751938
134774083547740859TGTGTGTGTGTGTGTGTGTGTGTG------------------------7GENIChomozygous49751939
134774100347741004CT23GENIChomozygous49751940
134774103147741032TC19GENIChomozygous49751941
134774122747741228GA26GENIChomozygous49751942
134774150347741504CA22GENIChomozygous49751943
134774173447741735GT17GENIChomozygous49751944
134774190247741903GA13GENIChomozygous49751945
134774233347742355GTGTGTGTGTATGTGTGTGTGT----------------------21GENIChomozygous49751946
134774286247742863TC20GENIChomozygous49751950
134774287247742873GA20GENIChomozygous49751951
134774288347742884AG21GENIChomozygous49751952
134774295147742952GA30GENIChomozygous49751953
134774306747743068C-17GENIChomozygous49751954
134774326947743270GT27GENIChomozygous49751955
134774334847743349AG26GENIChomozygous49751956
134774335547743356AC30GENIChomozygous49751957