chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6136367144136367145AT61GENIChomozygous118556380
6136367145136367146TC61GENIChomozygous115082209
6136367508136367509GA70GENIChomozygous114994881
6136367802136367803TC71GENIChomozygous114994882
6136367888136367889CT81GENIChomozygous114994883
6136367891136367892TC81GENIChomozygous114994884
6136368176136368177TG69GENIChomozygous114994885
6136368755136368756GT66GENIChomozygous114994886
6136369393136369394GA68GENIChomozygous114994887
6136369727136369728TC70GENIChomozygous114994888
6136369954136369955AG62GENIChomozygous114994889
6136370078136370079TC55GENIChomozygous114994890
6136370100136370101TC55GENIChomozygous114994891
6136370105136370106GA60GENIChomozygous114994892
6136370522136370523TC63GENIChomozygous114994893
6136370591136370592GA62GENIChomozygous114994894
6136369054136369058GTTT53GENIChomozygous128400080
6136371131136371132GA75GENIChomozygous114994895
6136371165136371166AG69GENIChomozygous114994896
6136371211136371212GT66GENICpossibly homozygous114994897
6136371224136371228GTGT57GENIChomozygous128400081
6136371817136371818CT68GENIChomozygous114994898
6136372055136372056TC78GENIChomozygous114994899
6136372300136372301CT65GENIChomozygous114994900
6136372602136372602AGG68GENIChomozygous128400082
6136372655136372656GA75GENIChomozygous114994901
6136372927136372928GA71GENIChomozygous114994902
6136372933136372934CT73GENIChomozygous114994903
6136372999136373000AG72GENIChomozygous114994904
6136373092136373093CT69GENIChomozygous114994905
6136380598136380599CT59GENIChomozygous114994906