chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124494318244943183GA49GENIChomozygous115391862
124494374344943744CT51GENIChomozygous115391864
124494388144943882CG53GENIChomozygous115338585
124494464544944646AC49GENIChomozygous115338595
124494465744944658AG50GENIChomozygous115391866
124494480544944806GA63GENIChomozygous115391868
124494565144945652AG32GENICheterozygous115511593
124494565544945656AG33GENICheterozygous115391870
124494566344945664GA38GENICheterozygous115391872
124494621544946216GA40GENIChomozygous115391874
124494673244946733AG35GENICpossibly homozygous115338627
124494828844948289TC43GENIChomozygous115338635
124494847544948476TC51GENICpossibly homozygous115338639
124494988844949889CG44GENIChomozygous115338657
124495036044950361AG41GENIChomozygous115391876
124495193344951934AG59GENIChomozygous115391878
124495198944951990AG49GENIChomozygous115391880
124495358244953583AG42GENIChomozygous115338675
124495370644953707TC49GENIChomozygous115338677
124495383544953836GA37GENIChomozygous115391882
124495424044954241CT52GENIChomozygous115391884
124495433244954333CA70GENICpossibly homozygous115391886
124495477244954773GC10GENIChomozygous118271956
124495481844954819GA13GENICheterozygous118306001
124495518744955188AG59GENIChomozygous115338685
124495548744955488GA44GENIChomozygous115391888
124495563644955637AT40GENICheterozygous115566789
124495753644957537CT39GENIChomozygous115391890
124495764044957641CT51GENIChomozygous115391892
124495832044958321GA30GENIChomozygous115391894
124495849344958494TA28GENIChomozygous115451922
124496003444960035GA46GENIChomozygous115338723
124496036244960363TC33GENIChomozygous115338725
124496079944960800GA20GENICheterozygous118306003
124496121644961217TA39GENIChomozygous115338734
124496213244962133GT47GENIChomozygous115391896
124496224044962241CT41GENICpossibly homozygous115391898
124496234044962341TC20GENIChomozygous115391900