chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174368058343680584TC36GENIChomozygous111053499
174368089743680898AG31GENIChomozygous111053501
174368099943681000CT36GENIChomozygous111053503
174368164843681649GA36GENIChomozygous111053510
174368164943681650CA36GENIChomozygous111053512
174368165643681657GA36GENIChomozygous111053514
174368245143682452CG45GENIChomozygous111053516
174368338343683384TC30GENIChomozygous111053518
174368398043683981CA35GENIChomozygous111053520
174368436843684369TC19GENIChomozygous111053522
174368438643684387CA14GENIChomozygous111053524
174368542743685428TC33GENICpossibly homozygous119286370
174368587443685875GT49GENICheterozygous119286371
174368669243686693TC23GENICpossibly homozygous111053526
174368673643686737TC15GENIChomozygous111053528
174368684743686848AG16GENIChomozygous111053530
174368693543686936TC8GENIChomozygous111053532
174368777143687772GT38GENIChomozygous111053534
174368781743687818AC36GENIChomozygous111053536
174368873743688738CA27GENIChomozygous111053538
174368874943688750GA30GENIChomozygous111053540
174368893443688935TC40GENIChomozygous119286372
174368901243689013GA57GENIChomozygous119286373
174368922543689226GC47GENIChomozygous111053542
174368923143689232AT45GENIChomozygous111053544