chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18157242881572429GT17GENIChomozygous559731843
18157252381572524TA17GENIChomozygous559731844
18157273481572735AG19GENIChomozygous559731845
18157443181574432TC22GENIChomozygous561861420
18157497481574975GA23GENIChomozygous559731846
18157525781575258CA29GENIChomozygous559731847
18157600881576009TC17GENIChomozygous559731848
18157693481576935TC15GENIChomozygous559731849
18157693981576941AC--1GENIChomozygous705602401
18157825881578259CA15GENIChomozygous559731850
18157829981578300CCTT13GENIChomozygous705602402
18157831981578320AAC17GENIChomozygous705602403
18157871181578712GA26GENIChomozygous561861421
18157879381578794TC26GENIChomozygous559731851
18157896081578961AG19GENIChomozygous561861422
18157923181579232AG14GENIChomozygous559731852
18157977781579789GTATGCATGTGC------------4GENICheterozygous705602404
18158000381580004A-20GENICheterozygous705602406
18158035581580356A-8GENIChomozygous705602407
18158083381580834C-25GENIChomozygous705602408
18158108781581088AAAC18GENICpossibly homozygous705602411
18158127081581271AG26GENIChomozygous559731853
18158139781581398C-15GENIChomozygous705602413
18158206781582068GC4GENIChomozygous559731854
18158212681582127GC3GENIChomozygous561861423