chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123942911339429114T-14GENICheterozygous50543028
123942912439429125AAT11GENICheterozygous50571299
123942915939429160GGT5GENICheterozygous50199241
123942916039429162TT--5GENICheterozygous50199243
123942917439429176TT--5GENICheterozygous50199245
123943170039431701AT24GENIChomozygous50511687
123943253639432549AGAAAAAAAAAAG-------------7GENICheterozygous50543030
123943380939433810A-18GENIChomozygous50199261
123943421739434218CA35GENIChomozygous50199263
123943426639434267GGT19GENIChomozygous50199265
123943522239435223GA30GENIChomozygous50511689
123943598739435988GC11GENIChomozygous50571301
123943602639436031GAACC-----2GENIChomozygous50199271
123943691939436920CG12GENIChomozygous50571302
123943696539436966A-11GENICheterozygous50199275
123943839839438399TC18GENIChomozygous50199279
123944005639440062AAAAAG------9GENIChomozygous50511691
123944043239440433GA19GENIChomozygous50511693
123944048239440483CG16GENIChomozygous50199292
123944102439441025TA26GENIChomozygous50511695
123944199239441993GGT20GENIChomozygous50199300
123944225539442258AAA---9GENIChomozygous50571304
123944307039443074TAAC----29GENIChomozygous50511699
123944307439443075AATT27GENIChomozygous50511701
123944357439443575GA25GENIChomozygous50511703
123944539039445391AG9GENIChomozygous50199314
123944539739445398TTG7GENIChomozygous50511705
123944746639447469AAA---16GENICheterozygous50412826
123944746739447469AA--16GENICheterozygous50543034
123944746839447469A-16GENICheterozygous50451970
123944791139447919TATTTATT--------2GENIChomozygous50571306
123945073239450733GGAAAAAAA5GENICheterozygous50199334
123945073239450733GGAAAAAA5GENICheterozygous50543036
123945093939450940GGA10GENICpossibly homozygous50199338
123945093939450940GGAA10GENICheterozygous50558896