chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134773940047739401AC48GENIChomozygous49751928
134773962347739624TC36GENIChomozygous49751929
134773965547739656TC40GENIChomozygous49751930
134774008847740089CT29GENIChomozygous49751931
134774031347740314GA34GENIChomozygous49751932
134774035847740359AG30GENIChomozygous49751933
134774037447740375AG30GENIChomozygous49751934
134774037647740377GA32GENIChomozygous49751935
134774052647740527TC31GENICpossibly homozygous49751936
134774052947740530AC30GENICpossibly homozygous49751937
134774078747740788AG40GENIChomozygous49751938
134774083547740859TGTGTGTGTGTGTGTGTGTGTGTG------------------------6GENIChomozygous49751939
134774100347741004CT43GENIChomozygous49751940
134774103147741032TC31GENIChomozygous49751941
134774122747741228GA56GENIChomozygous49751942
134774150347741504CA34GENIChomozygous49751943
134774173447741735GT50GENIChomozygous49751944
134774190247741903GA44GENIChomozygous49751945
134774233347742355GTGTGTGTGTATGTGTGTGTGT----------------------22GENICpossibly homozygous49751946
134774234147742342GGCA27GENICheterozygous49751947
134774234347742344AATGTG18GENICheterozygous49751948
134774234447742346TG--18GENICheterozygous49751949
134774286247742863TC45GENIChomozygous49751950
134774287247742873GA40GENICpossibly homozygous49751951
134774288347742884AG37GENIChomozygous49751952
134774295147742952GA39GENIChomozygous49751953
134774306747743068C-30GENIChomozygous49751954
134774326947743270GT30GENIChomozygous49751955
134774334847743349AG59GENIChomozygous49751956
134774335547743356AC61GENIChomozygous49751957