chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134773940047739401AC31GENIChomozygous49751928
134773962347739624TC22GENIChomozygous49751929
134773965547739656TC28GENIChomozygous49751930
134774008847740089CT24GENIChomozygous49751931
134774031347740314GA25GENIChomozygous49751932
134774035847740359AG27GENIChomozygous49751933
134774037447740375AG30GENIChomozygous49751934
134774037647740377GA30GENIChomozygous49751935
134774052647740527TC35GENIChomozygous49751936
134774052947740530AC34GENIChomozygous49751937
134774078747740788AG19GENIChomozygous49751938
134774083547740859TGTGTGTGTGTGTGTGTGTGTGTG------------------------17GENIChomozygous49751939
134774100347741004CT22GENIChomozygous49751940
134774103147741032TC23GENIChomozygous49751941
134774122747741228GA24GENIChomozygous49751942
134774150347741504CA25GENIChomozygous49751943
134774173447741735GT16GENIChomozygous49751944
134774190247741903GA37GENIChomozygous49751945
134774233347742355GTGTGTGTGTATGTGTGTGTGT----------------------23GENIChomozygous49751946
134774286247742863TC28GENIChomozygous49751950
134774287247742873GA26GENIChomozygous49751951
134774288347742884AG27GENIChomozygous49751952
134774295147742952GA14GENIChomozygous49751953
134774306747743068C-26GENICpossibly homozygous49751954
134774326947743270GT25GENICpossibly homozygous49751955
134774334847743349AG30GENIChomozygous49751956
134774335547743356AC30GENIChomozygous49751957