chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421645514216456CA21GENIChomozygous51622873
101421707914217080A-21GENIChomozygous51622874
101421825814218259TG18GENIChomozygous51622875
101421860014218601TC17GENIChomozygous51329145
101421890814218909CT26GENIChomozygous51622876
101421947314219474AG28GENIChomozygous51622877
101421964814219649AT32GENIChomozygous51622878
101421978914219790TC21GENIChomozygous51622879
101422006114220062TC24GENIChomozygous51622880
101422119314221194TC21GENIChomozygous51622881
101422235314222354GA8GENIChomozygous51622882
101422348314223484GA27GENIChomozygous51622883
101422363814223639GA22GENIChomozygous51622884
101422370514223706C-10GENIChomozygous51622885
101422402414224025CT27GENIChomozygous51622886
101422447614224477CCT16GENICheterozygous51329146
101422447614224477CCTTTTT16GENICheterozygous51329147
101422567014225671GA17GENIChomozygous51622888
101422631914226320T-21GENIChomozygous51622889
101422709614227097TC13GENIChomozygous51622890
101422711614227117CCT7GENICheterozygous51622891
101422711714227118T-7GENICheterozygous51810360
101422714414227145CCT3GENIChomozygous51622892
101422803014228031AC24GENIChomozygous51622893
101422806814228077GTGCAATGA---------13GENIChomozygous51622894
101422831014228311TC16GENIChomozygous51622895
101422932814229329TG18GENIChomozygous51622896
101422937114229372GA23GENIChomozygous51622897
101422967714229678GA21GENIChomozygous51622898
101423004714230073TGTGTGTGTGTGTGTGTGTGTGTGGT--------------------------6GENIChomozygous52481347