chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421645514216456CA32GENIChomozygous51622873
101421707914217080A-23GENIChomozygous51622874
101421825814218259TG22GENICpossibly homozygous51622875
101421860014218601TC16GENIChomozygous51329145
101421890814218909CT39GENIChomozygous51622876
101421947314219474AG27GENIChomozygous51622877
101421964814219649AT21GENIChomozygous51622878
101421978914219790TC24GENIChomozygous51622879
101422006114220062TC41GENIChomozygous51622880
101422119314221194TC29GENIChomozygous51622881
101422235314222354GA17GENIChomozygous51622882
101422348314223484GA29GENIChomozygous51622883
101422363814223639GA31GENIChomozygous51622884
101422370514223706C-31GENIChomozygous51622885
101422402414224025CT36GENIChomozygous51622886
101422447614224477CCT11GENICheterozygous51329146
101422447614224477CCTTTTT11GENICheterozygous51329147
101422567014225671GA20GENIChomozygous51622888
101422631914226320T-30GENIChomozygous51622889
101422709614227097TC9GENIChomozygous51622890
101422711614227117CCT2GENIChomozygous51622891
101422714414227145CCT2GENIChomozygous51622892
101422803014228031AC22GENIChomozygous51622893
101422937114229372GA36GENIChomozygous51622897
101422806814228077GTGCAATGA---------15GENIChomozygous51622894
101422831014228311TC27GENIChomozygous51622895
101422932814229329TG33GENIChomozygous51622896
101422967714229678GA35GENIChomozygous51622898
101423004714230073TGTGTGTGTGTGTGTGTGTGTGTGGT--------------------------13GENICheterozygous52481347