chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94333340143333405TGTG----6GENIChomozygous52388130
94334010743340108CCTGTG12GENIChomozygous51933497
94334481243344813AAT22GENIChomozygous52181824
94334500143345002GA24GENIChomozygous52181826
94334500343345004TC25GENIChomozygous52181829
94334501443345015GA23GENIChomozygous52181831
94334523143345232AT21GENIChomozygous52181833
94334525443345255GA24GENIChomozygous52181836
94334534743345348AG24GENIChomozygous52181838
94334539943345400AC27GENIChomozygous52181841
94334545843345459TC32GENIChomozygous52181843
94334563943345640TC20GENIChomozygous52181846
94334591243345913TC20GENIChomozygous52181848
94334602243346023TTG24GENIChomozygous52181851
94334624043346241CT28GENIChomozygous52181853
94334641443346415TTA18GENIChomozygous52181856
94334703343347034CA23GENIChomozygous52181858
94334716843347169GA15GENIChomozygous52181861
94334850943348510TTACTA28GENIChomozygous52181864
94334858743348588GGTT17GENICpossibly homozygous52906034
94334921343349214CT19GENIChomozygous52181869
94334960843349609TTGGG10GENIChomozygous53190713
94335036643350367TC16GENIChomozygous52181874
94335065543350656GA25GENIChomozygous52181876
94335086643350867CT21GENIChomozygous52181878
94335093543350936TC10GENIChomozygous52181881
94335100143351002TC14GENIChomozygous52181883
94335170843351709AG22GENIChomozygous52181886
94335171343351714GA22GENIChomozygous52181889
94335206943352070AC14GENIChomozygous52181891
94335224243352243TC33GENIChomozygous52181894