chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47098051370980514CT66GENIChomozygous112703870
47098194770981948CT69GENIChomozygous112703872
47098341470983414T56GENIChomozygous128047426
47098385970983860CT55GENIChomozygous112703874
47098402870984029TC62GENIChomozygous112703876
47098421670984217AT51GENIChomozygous112703878
47098422570984226TC51GENIChomozygous112703880
47098423370984234TC53GENIChomozygous112703882
47098425270984253AT62GENIChomozygous112703884
47098478070984781AT52GENIChomozygous112703886
47098589870985905TGAAGGC43GENIChomozygous128047427
47098596970985970GC41GENIChomozygous112703888
47098628170986282CT55GENIChomozygous112703890
47098812870988129TA48GENIChomozygous112703892
47098821370988214TC47GENIChomozygous112703894
47098847570988476CG50GENIChomozygous112703896
47098852070988521GA48GENIChomozygous112703898
47098933770989338CT59GENIChomozygous112703900
47098953070989531GA70GENIChomozygous112703902
47099042970990430GA75GENICpossibly homozygous112703904
47099081870990819CT56GENIChomozygous112703906
47099131370991313T57GENIChomozygous128047428
47099145070991450AAAC45GENIChomozygous128047429
47099179270991793CA56GENIChomozygous112703908
47099186770991868AG55GENIChomozygous112703910
47099205770992057GGTAAAA50GENIChomozygous128047430
47099283470992835TG39GENICpossibly homozygous112703912
47099346670993467CA48GENIChomozygous112703914
47099349770993498GA53GENIChomozygous112703916
47099394270993943TC53GENIChomozygous112703918
47099399770993998AG62GENIChomozygous112703920
47099417070994171TG63GENIChomozygous112703922
47099439470994395C77GENIChomozygous128047431
47099483370994834CT66GENIChomozygous112703924
47099499570994996T61GENIChomozygous128047432
47099510570995106TC52GENIChomozygous112703926
47099551170995512TC55GENIChomozygous112703928
47099603570996036CG47GENIChomozygous112703930
47099625270996253CT56GENIChomozygous112703932
47099627670996277TC53GENIChomozygous112703934
47099669270996693TC52GENIChomozygous112703936