chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167409832974098330TC59INTERGENIChomozygous47524427
167409860774098608GA55INTERGENIChomozygous47697484
167409885274098853CA30INTERGENICheterozygous47524431
167409886674098867CT25INTERGENICpossibly homozygous47697485
167409895374098954AG56INTERGENICpossibly homozygous47697486
167409901874099019TC55INTERGENIChomozygous47524435
167409960774099608AG14INTERGENIChomozygous47697487
167410363674103637A-43GENIChomozygous47524441
167410381174103812TC47GENICpossibly homozygous47524443
167410481574104816AG52GENICpossibly homozygous47524445
167410503974105040TC45GENIChomozygous47697488
167410553774105538AAG53GENIChomozygous47524447
167411673674116737GA57GENICpossibly homozygous47524449
167411689374116894GA75GENIChomozygous47697489
167411819774118198GA65GENIChomozygous47697490
167411904974119050TC65GENICpossibly homozygous47697491
167411910374119104TC54GENICpossibly homozygous47697492
167411925474119255CA46GENIChomozygous47697493
167411935974119360AG47GENIChomozygous47697494
167411950974119510CG50GENIChomozygous47697495
167412026974120270AT62GENIChomozygous47697496
167412053474120535AG55GENIChomozygous47697497
167412087074120871TC56GENIChomozygous47697498
167412092474120925CT52GENIChomozygous47697499
167412117974121180AG37GENIChomozygous47697500
167412128074121281AG49GENIChomozygous47524451
167412165474121655TA66GENICpossibly homozygous47697501
167412173774121738TC47GENICpossibly homozygous47697502
167412194874121949CT74GENICpossibly homozygous47697503
167412218174122182CT30GENIChomozygous47697504
167412218974122190GA35GENICheterozygous47697505
167412218974122190GGAGAGCTTCATA35GENIChomozygous47697506
167412248674122487GA46GENIChomozygous47697507
167412253974122540AG51GENIChomozygous47697508
167412255474122555GA58GENIChomozygous47697509
167412256374122564TC57GENIChomozygous47697510
167412285274122856GGAG----47GENIChomozygous47697511