chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421645514216456CA16GENIChomozygous51622873
101421707914217080A-23GENIChomozygous51622874
101421825814218259TG16GENIChomozygous51622875
101421860014218601TC10GENIChomozygous51329145
101421881514218816GC14GENICheterozygous53505999
101421881814218819TG15GENICheterozygous53506001
101421884114218842TC17GENICheterozygous53506003
101421890814218909CT11GENIChomozygous51622876
101421947314219474AG16GENIChomozygous51622877
101421964814219649AT25GENIChomozygous51622878
101421978914219790TC12GENIChomozygous51622879
101422006114220062TC17GENIChomozygous51622880
101422119314221194TC15GENIChomozygous51622881
101422235314222354GA15GENIChomozygous51622882
101422348314223484GA24GENIChomozygous51622883
101422363814223639GA23GENIChomozygous51622884
101422370514223706C-16GENIChomozygous51622885
101422402414224025CT14GENIChomozygous51622886
101422567014225671GA14GENIChomozygous51622888
101422631914226320T-17GENIChomozygous51622889
101422709614227097TC9GENIChomozygous51622890
101422803014228031AC17GENIChomozygous51622893
101422806814228077GTGCAATGA---------12GENIChomozygous51622894
101422831014228311TC10GENIChomozygous51622895
101422932814229329TG11GENIChomozygous51622896
101422937114229372GA14GENIChomozygous51622897
101422967714229678GA9GENIChomozygous51622898