chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761598617615987TC13GENIChomozygous991859897
141761702817617029CA5GENIChomozygous991859898
141762106317621064TC22GENIChomozygous991859899
141762138217621383TC12GENIChomozygous991859900
141762256517622566TA21GENIChomozygous991859901
141762303117623032CT18GENIChomozygous991859902
141762436417624365CT22GENIChomozygous991859903
141762439017624391TC24GENIChomozygous991859904
141762442617624427CG21GENIChomozygous991859905
141762588517625886AG17GENIChomozygous991859906
141762981017629811AG20GENIChomozygous991859907
141762983717629838TC20GENIChomozygous991859908
141762984117629842TC19GENIChomozygous991859909
141762992517629926AG20GENIChomozygous991859910
141763052217630523TA19GENIChomozygous991859911
141763065017630651TG22GENIChomozygous991859912