chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
24545505645455057AC25GENIChomozygous110693502
24545529045455291TC30GENIChomozygous120167514
24545604245456043TG16GENIChomozygous110693504
24545634045456341CT23GENIChomozygous110693506
24545635545456356TC22GENIChomozygous109728600
24545720445457205TC19GENIChomozygous109728604
24545811445458115GA23GENIChomozygous110693510
24545826045458261CT16GENIChomozygous110693512
24545837045458371GA20GENIChomozygous110693514
24545871345458714GA20GENIChomozygous109728606
24545936245459363CT16GENIChomozygous109728609
24546061145460612CA17GENIChomozygous110693516
24546222245462223GT33GENIChomozygous109728613
24546232945462330AG22GENIChomozygous110693520
24546437745464378TC24GENIChomozygous110693522
24546447745464478TC31GENIChomozygous110693524
24546531445465315CG19GENIChomozygous110693526
24546607645466077CA17GENIChomozygous110693532
24546684345466844GC17GENIChomozygous110693534
24546720745467208CG6GENIChomozygous110693536
24546791745467918CT11GENIChomozygous110693538
24546798745467988TC16GENIChomozygous109728615
24547026945470270AG17GENIChomozygous120167517
24547037345470374CT27GENIChomozygous110693540
24547039945470400GA27GENIChomozygous120167518
24547205245472053AG29GENIChomozygous110693547
24547267145472672AG36GENIChomozygous120167519
24547366045473661CT10GENIChomozygous120167520
24547455845474559AG15GENIChomozygous109728621
24547466045474661TC16GENIChomozygous110509449
24547507945475080AC8GENIChomozygous109728623
24547511345475114AC12GENIChomozygous109728625
24547533245475333TC16GENIChomozygous109728627
24547549345475494AG15GENIChomozygous110509450
24547578745475788GC18GENIChomozygous109728639
24547770345477704CT29GENIChomozygous110509451
24547806745478068AG16GENIChomozygous120167521
24547917245479173GA7GENIChomozygous120167522
24548079445480795CT5GENIChomozygous120167523