chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47098051370980514CT41GENIChomozygous112703870
47098194770981948CT60GENIChomozygous112703872
47098385970983860CT61GENIChomozygous112703874
47098402870984029TC53GENIChomozygous112703876
47098421670984217AT41GENIChomozygous112703878
47098422570984226TC44GENIChomozygous112703880
47098423370984234TC42GENIChomozygous112703882
47098425270984253AT45GENIChomozygous112703884
47098478070984781AT44GENIChomozygous112703886
47098596970985970GC23GENIChomozygous112703888
47098628170986282CT42GENIChomozygous112703890
47098812870988129TA31GENIChomozygous112703892
47098821370988214TC34GENIChomozygous112703894
47098847570988476CG27GENIChomozygous112703896
47098852070988521GA35GENIChomozygous112703898
47098933770989338CT45GENIChomozygous112703900
47098953070989531GA50GENIChomozygous112703902
47099042970990430GA57GENIChomozygous112703904
47099081870990819CT45GENIChomozygous112703906
47099179270991793CA40GENIChomozygous112703908
47098341470983414T47GENIChomozygous128047426
47098589870985905TGAAGGC32GENIChomozygous128047427
47099131370991313T50GENIChomozygous128047428
47099145070991450AAAC32GENIChomozygous128047429
47099186770991868AG37GENIChomozygous112703910
47099205770992057GGTAAAA34GENIChomozygous128047430
47099283470992835TG43GENIChomozygous112703912
47099346670993467CA60GENIChomozygous112703914
47099349770993498GA59GENIChomozygous112703916
47099394270993943TC46GENIChomozygous112703918
47099399770993998AG46GENIChomozygous112703920
47099439470994395C40GENIChomozygous128047431
47099499570994996T57GENIChomozygous128047432
47099510570995106TC63GENIChomozygous112703926
47099417070994171TG56GENIChomozygous112703922
47099483370994834CT63GENIChomozygous112703924
47099551170995512TC46GENIChomozygous112703928
47099603570996036CG51GENIChomozygous112703930
47099625270996253CT39GENIChomozygous112703932
47099627670996277TC39GENIChomozygous112703934
47099669270996693TC42GENIChomozygous112703936