chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1043157324315733TC21GENIChomozygous126374499
1043161784316179CT23GENIChomozygous126374500
1043181784318179GA16GENIChomozygous126374502
1043211384321139GC12GENIChomozygous126472418
1043220424322043TG9GENIChomozygous126374507
1043232094323210CT8GENIChomozygous126472419
1043261294326130CT17GENIChomozygous126455633
1043264604326461TC15GENIChomozygous126374513
1043274714327472GA13GENIChomozygous126455634
1043289914328992AG16GENIChomozygous126374516
1043310134331014TG17GENIChomozygous126374517
1043333014333302AG17GENIChomozygous126374521
1043338674333868GA25GENIChomozygous126472420
1043345654334566TC16GENIChomozygous126374525
1043346514334652GT16GENIChomozygous126374527
1043351824335183AG12GENIChomozygous126374528
1043361334336134GA6GENIChomozygous126374529
1043369904336991CT15GENIChomozygous126472421
1043370774337078GC18GENIChomozygous126374530
1043370914337092CT14GENIChomozygous126472422
1043394484339449CT10GENIChomozygous126472423
1043413634341364GA16GENIChomozygous126472424
1043417534341754AG10GENIChomozygous126374533
1043437684343769CG20GENIChomozygous126374534
1043442794344280AG12GENICheterozygous126472425
1043443584344359GT16GENIChomozygous126374535
1043449704344971GA28GENIChomozygous126374536
1043457064345707TC15GENIChomozygous126472426