chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44457327644573277GC17GENIChomozygous112619284
44457337244573373CG27GENIChomozygous112619286
44457340144573402CT26GENIChomozygous112619288
44457346844573469GA17GENIChomozygous112619290
44457369244573693CG22GENIChomozygous112619292
44457414744574148TC16GENIChomozygous112619294
44457415544574156CG17GENIChomozygous112619296
44457435944574359T6GENIChomozygous128027933
44457437544574375G4GENIChomozygous128027934
44457443844574439GT8GENICpossibly homozygous112619298
44457488244574883CT21GENIChomozygous112619300
44457514244575143CT23GENIChomozygous112619302
44457518144575188GCCCATC22GENIChomozygous128027935
44457552644575527TC18GENIChomozygous112619304
44457560344575604GA19GENIChomozygous112619306
44457563844575639GA21GENIChomozygous112619308
44457612644576126T22GENIChomozygous128027938
44457550344575503T20GENICpossibly homozygous128027936
44457572744575727A29GENICpossibly homozygous128027937
44457801844578018A14GENIChomozygous128027939
44457843644578437CG20GENICpossibly homozygous112619310
44458024944580250CG25GENIChomozygous112619312
44458056544580577GAAACTTTTACT17GENIChomozygous128027940