chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421645514216456CA29GENIChomozygous51622873
101421707914217080A-25GENIChomozygous51622874
101421825814218259TG30GENIChomozygous51622875
101421860014218601TC32GENIChomozygous51329145
101421890814218909CT30GENIChomozygous51622876
101421947314219474AG36GENIChomozygous51622877
101421964814219649AT44GENIChomozygous51622878
101421978914219790TC38GENIChomozygous51622879
101422006114220062TC24GENIChomozygous51622880
101422119314221194TC21GENIChomozygous51622881
101422235314222354GA24GENIChomozygous51622882
101422348314223484GA29GENIChomozygous51622883
101422363814223639GA32GENIChomozygous51622884
101422370514223706C-27GENIChomozygous51622885
101422402414224025CT36GENIChomozygous51622886
101422447614224477CCT20GENICheterozygous51329146
101422447614224477CCTTTTT20GENICheterozygous51329147
101422567014225671GA31GENIChomozygous51622888
101422631914226320T-31GENIChomozygous51622889
101422709614227097TC18GENIChomozygous51622890
101422711614227117CCT12GENICheterozygous51622891
101422711714227118T-12GENICheterozygous51810360
101422714414227145CCT17GENIChomozygous51622892
101422803014228031AC25GENIChomozygous51622893
101422806814228077GTGCAATGA---------21GENIChomozygous51622894
101422831014228311TC21GENIChomozygous51622895
101422932814229329TG20GENIChomozygous51622896
101422937114229372GA31GENIChomozygous51622897
101422967714229678GA39GENIChomozygous51622898
101423004714230073TGTGTGTGTGTGTGTGTGTGTGTGGT--------------------------14GENICheterozygous52481347