chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133819822133819823TA13GENIChomozygous114531637
5133820300133820301AG16GENIChomozygous114015074
5133820671133820672GA17GENIChomozygous114531639
5133820719133820720TG14GENIChomozygous114015076
5133822247133822248GA20GENIChomozygous114015078
5133824201133824202GT10GENIChomozygous114531645
5133824212133824213CT10GENIChomozygous114531647
5133825125133825126TC26GENIChomozygous114531649
5133827219133827220AG14GENIChomozygous114015080
5133827290133827291GA15GENIChomozygous114015081
5133827386133827387CT14GENIChomozygous114531651
5133828333133828334CT8GENIChomozygous114531653
5133829155133829156TC11GENIChomozygous114015083
5133822925133822927TC11GENIChomozygous132844042
5133832156133832156A6GENIChomozygous132844043
5133835965133835966GA8GENIChomozygous114531655
5133836418133836419AC9GENIChomozygous114015095
5133837094133837095CT13GENIChomozygous114531659
5133837152133837152CCTCTGC10GENIChomozygous132844044
5133838989133838990AG13GENIChomozygous114015099
5133841631133841632C10GENIChomozygous130962512
5133842154133842154AAC7GENIChomozygous130962513
5133843480133843481GA17GENIChomozygous114531661
5133844463133844464GC9GENIChomozygous114531663
5133845526133845527GA19GENIChomozygous114531665
5133846062133846063GA16GENIChomozygous114143364
5133846071133846071TATA13GENIChomozygous132844045
5133846760133846761AG15GENIChomozygous114015112
5133846847133846848GT10GENIChomozygous114531667
5133848389133848389GTGA24GENICpossibly homozygous128241318
5133848392133848393TA25GENICheterozygous126312402
5133849451133849452AG16GENIChomozygous114015118
5133849923133849924CT16GENIChomozygous114531669
5133850405133850406AG28GENIChomozygous114015120
5133850563133850564TC17GENIChomozygous114015121
5133850937133850938AG18GENIChomozygous114015123
5133850996133850997GC18GENIChomozygous114015124
5133851281133851282GA18GENIChomozygous114015125
5133851274133851275AT20GENIChomozygous118858406
5133848398133848399TC25GENICheterozygous130971669