chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31806249118062492TC58GENIChomozygous143019898
31806825818068259AG82GENIChomozygous143019899
31806911118069112CT47GENICpossibly homozygous143019901
31807043918070440AT42GENIChomozygous143019902
31807053218070533AG46GENIChomozygous143019904
31807170518071706AG46GENIChomozygous143019905
31807202218072023AG20GENIChomozygous136647282
31807204018072040GGAA18GENIChomozygous144627781
31807204818072048GGAA19GENIChomozygous144627782
31807223918072240GA35GENIChomozygous143019906
31807290318072904TC34GENIChomozygous143019907
31807297518072976GA27GENIChomozygous143019908
31807457418074575AG36GENIChomozygous136647283
31807489918074900CG14GENIChomozygous143019910
31807490218074902GGC13GENIChomozygous143000604
31807490818074908AG8GENIChomozygous143000605
31807491318074916CAG7GENIChomozygous143000606
31807492918074933CCGA3GENIChomozygous143000607
31807493718074937TAA3GENIChomozygous143000608
31807494118074947CCTGAG3GENIChomozygous143000609
31807494918074950C3GENIChomozygous143000610
31807551418075515GA49GENIChomozygous143019911
31807554318075544GA46GENIChomozygous143019912
31807557718075578AG45GENIChomozygous143019913
31807653618076537CA54GENIChomozygous136647285
31807669318076694CG49GENIChomozygous144635982
31807976518079766CT44GENIChomozygous144635983
31807995018079951GA34GENIChomozygous144635984
31808031218080313CT45GENIChomozygous136647289
31808088218080883GA44GENIChomozygous136647291
31808218818082216GCCTCCCGAGTGGTGCTAGGCTTTGCCT34GENIChomozygous144627783
31807939018079393GAA52GENIChomozygous136550666