chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161909741119097412GA40GENIChomozygous973964902
161909779819097799CT34GENIChomozygous973964903
161909817519098176GT21GENIChomozygous973964904
161909930319099304TA26GENIChomozygous973964905
161909955919099560AG31GENIChomozygous973964906
161909976019099761AG17GENIChomozygous973964907
161909977219099773TC19GENIChomozygous973964908
161909983319099834TC24GENIChomozygous973964909
161909990219099903GA33GENIChomozygous973964910
161910008019100081CT24GENIChomozygous973964911
161910045619100457CT16GENIChomozygous973964912
161910156819101569GA24GENIChomozygous973964913
161910184519101846TC21GENIChomozygous973964914
161910255019102551TG16GENIChomozygous973964915
161910344019103441CA19GENIChomozygous973964916
161910530319105304TC21GENIChomozygous973964917
161911392519113926CT19GENIChomozygous973964918
161911547419115475TC16GENIChomozygous973964919
161911899219118993CT19GENIChomozygous973964920
161911913719119138GA12GENIChomozygous973964921
161912265619122657TA16GENIChomozygous973964922
161912367519123676AC25GENIChomozygous973964923