chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47098051370980514CT47GENIChomozygous112703870
47098194770981948CT71GENIChomozygous112703872
47098341470983414T43GENIChomozygous128047426
47098385970983860CT52GENIChomozygous112703874
47098402870984029TC57GENICpossibly homozygous112703876
47098421670984217AT66GENIChomozygous112703878
47098422570984226TC68GENIChomozygous112703880
47098423370984234TC64GENIChomozygous112703882
47098425270984253AT55GENIChomozygous112703884
47098478070984781AT53GENICpossibly homozygous112703886
47098589870985905TGAAGGC37GENIChomozygous128047427
47098596970985970GC23GENIChomozygous112703888
47098628170986282CT37GENICpossibly homozygous112703890
47098812870988129TA44GENIChomozygous112703892
47098821370988214TC51GENIChomozygous112703894
47098847570988476CG53GENIChomozygous112703896
47098852070988521GA55GENIChomozygous112703898
47098933770989338CT46GENIChomozygous112703900
47098953070989531GA59GENIChomozygous112703902
47099042970990430GA50GENIChomozygous112703904
47099081870990819CT55GENIChomozygous112703906
47099131370991313T55GENIChomozygous128047428
47099145070991450AAAC39GENIChomozygous128047429
47099179270991793CA51GENIChomozygous112703908
47099186770991868AG43GENIChomozygous112703910
47099205770992057GGTAAAA47GENIChomozygous128047430
47099283470992835TG42GENIChomozygous112703912
47099346670993467CA59GENIChomozygous112703914
47099349770993498GA53GENIChomozygous112703916
47099394270993943TC58GENIChomozygous112703918
47099399770993998AG53GENIChomozygous112703920
47099417070994171TG52GENIChomozygous112703922
47099439470994395C44GENIChomozygous128047431
47099483370994834CT45GENIChomozygous112703924
47099499570994996T38GENIChomozygous128047432
47099510570995106TC50GENIChomozygous112703926
47099551170995512TC50GENIChomozygous112703928
47099603570996036CG46GENIChomozygous112703930
47099625270996253CT39GENIChomozygous112703932
47099627670996277TC37GENIChomozygous112703934
47099669270996693TC35GENIChomozygous112703936