chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134773940047739401AC23GENICpossibly homozygous49751928
134773962347739624TC9GENIChomozygous49751929
134773965547739656TC21GENIChomozygous49751930
134774008847740089CT19GENICheterozygous49751931
134774031347740314GA24GENIChomozygous49751932
134774035847740359AG13GENIChomozygous49751933
134774037447740375AG11GENIChomozygous49751934
134774037647740377GA12GENICpossibly homozygous49751935
134774052647740527TC13GENIChomozygous49751936
134774052947740530AC15GENIChomozygous49751937
134774078747740788AG16GENICheterozygous49751938
134774100347741004CT24GENIChomozygous49751940
134774103147741032TC11GENIChomozygous49751941
134774122747741228GA14GENIChomozygous49751942
134774150347741504CA18GENICpossibly homozygous49751943
134774173447741735GT25GENIChomozygous49751944
134774190247741903GA21GENICpossibly homozygous49751945
134774233347742355GTGTGTGTGTATGTGTGTGTGT----------------------9GENICheterozygous49751946
134774286247742863TC10GENIChomozygous49751950
134774287247742873GA8GENIChomozygous49751951
134774288347742884AG7GENIChomozygous49751952
134774295147742952GA20GENICpossibly homozygous49751953
134774306747743068C-15GENIChomozygous49751954
134774326947743270GT22GENIChomozygous49751955
134774334847743349AG16GENIChomozygous49751956
134774335547743356AC15GENICpossibly homozygous49751957