chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421645514216456CA30GENIChomozygous51622873
101421707914217080A-21GENIChomozygous51622874
101421825814218259TG40GENIChomozygous51622875
101421860014218601TC36GENIChomozygous51329145
101421890814218909CT29GENIChomozygous51622876
101421947314219474AG19GENIChomozygous51622877
101421964814219649AT29GENIChomozygous51622878
101421978914219790TC16GENIChomozygous51622879
101422006114220062TC30GENIChomozygous51622880
101422119314221194TC31GENIChomozygous51622881
101422235314222354GA41GENIChomozygous51622882
101422348314223484GA28GENIChomozygous51622883
101422363814223639GA29GENIChomozygous51622884
101422370514223706C-36GENIChomozygous51622885
101422402414224025CT24GENIChomozygous51622886
101422447614224477CCT21GENICheterozygous51329146
101422447614224477CCTTTTT21GENICheterozygous51329147
101422567014225671GA40GENIChomozygous51622888
101422631914226320T-36GENIChomozygous51622889
101422709614227097TC16GENIChomozygous51622890
101422711614227117CCT15GENICheterozygous51622891
101422714414227145CCT19GENIChomozygous51622892
101422803014228031AC20GENIChomozygous51622893
101422806814228077GTGCAATGA---------21GENIChomozygous51622894
101422831014228311TC38GENIChomozygous51622895
101422932814229329TG43GENIChomozygous51622896
101422937114229372GA42GENIChomozygous51622897
101422967714229678GA38GENIChomozygous51622898
101423004714230073TGTGTGTGTGTGTGTGTGTGTGTGGT--------------------------21GENICpossibly homozygous52481347