chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167409832974098330TC21INTERGENIChomozygous47524427
167409860774098608GA19INTERGENIChomozygous47697484
167409885274098853CCACAA2INTERGENIChomozygous47951771
167409886674098867CT23INTERGENIChomozygous47697485
167409895374098954AG33INTERGENIChomozygous47697486
167409901874099019TC29INTERGENIChomozygous47524435
167409964574099675TCAGAGAAATAGTTTCCTGTCTGGAGTATC------------------------------4INTERGENIChomozygous48142302
167410139574101424ACCCAAGCCTGTGGACATTTTGGGGAAGG-----------------------------4INTERGENIChomozygous48142304
167410363674103637A-19GENIChomozygous47524441
167410381174103812TC17GENIChomozygous47524443
167410481574104816AG21GENIChomozygous47524445
167410503974105040TC23GENIChomozygous47697488
167410553774105538AAG11GENIChomozygous47524447
167411673674116737GA34GENIChomozygous47524449
167411689374116894GA26GENICpossibly homozygous47697489
167411819774118198GA25GENIChomozygous47697490
167411904974119050TC33GENIChomozygous47697491
167411910374119104TC28GENIChomozygous47697492
167411925474119255CA24GENIChomozygous47697493
167411935974119360AG30GENIChomozygous47697494
167411950974119510CG23GENIChomozygous47697495
167412026974120270AT38GENIChomozygous47697496
167412053474120535AG36GENIChomozygous47697497
167412087074120871TC23GENIChomozygous47697498
167412092474120925CT22GENIChomozygous47697499
167412117974121180AG18GENIChomozygous47697500
167412128074121281AG20GENIChomozygous47524451
167412165474121655TA24GENIChomozygous47697501
167412173774121738TC31GENIChomozygous47697502
167412194874121949CT30GENIChomozygous47697503
167412218174122182CT27GENIChomozygous47697504
167412218974122190GGAGAGCTTCATA26GENIChomozygous47697506
167412248674122487GA20GENIChomozygous47697507
167412253974122540AG26GENIChomozygous47697508
167412255474122555GA25GENIChomozygous47697509
167412256374122564TC25GENIChomozygous47697510
167412285274122856GGAG----16GENIChomozygous47697511
167412240874122409CCTTTTTTT18GENIChomozygous47945805