chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123942871739428718GGTCA30GENICheterozygous50543022
123942875839428759TTG24GENICheterozygous50543023
123942883239428833GGGGATCCTA19GENICheterozygous50543024
123942892339428933GTGTGGGCTT----------24GENICheterozygous50543025
123942893539428941TAATTT------20GENICheterozygous50543026
123942894139428942CCG19GENICheterozygous50543027
123942915939429160GGT7GENIChomozygous50199241
123942985439429870GTGTGTGTGTGTGTGT----------------4GENICheterozygous50907928
123942998139429982GGGTTA18GENICheterozygous50779067
123943253639432549AGAAAAAAAAAAG-------------8GENICheterozygous50543030
123943357839433588ACACACACAC----------16GENIChomozygous50946479
123943421739434218CA28GENIChomozygous50199263
123943426639434267GGT31GENIChomozygous50199265
123943532539435326TC23GENIChomozygous50946484
123943562239435623TC27GENIChomozygous50946487
123943602639436031GAACC-----5GENICheterozygous50199271
123943668439436685AG31GENICpossibly homozygous50946490
123943839839438399TC26GENIChomozygous50199279
123944048239440483CG24GENIChomozygous50199292
123944199239441993GGT33GENIChomozygous50199300
123944225439442255TTA15GENICheterozygous50199302
123944539039445391AG21GENIChomozygous50199314
123944539739445398TTG22GENIChomozygous50511705
123944746739447469AA--14GENIChomozygous50543034
123944759339447594AC27GENIChomozygous50946493
123945073239450733GGAAAAAA12GENIChomozygous50543036
123945093939450940GGA11GENICheterozygous50199338
123945093939450940GGAA11GENICheterozygous50558896