chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167409832974098330TC22INTERGENIChomozygous47524427
167409860774098608GA13INTERGENIChomozygous47697484
167409886674098867CT9INTERGENIChomozygous47697485
167409895374098954AG11INTERGENIChomozygous47697486
167409901874099019TC21INTERGENIChomozygous47524435
167410363674103637A-16GENIChomozygous47524441
167410381174103812TC13GENIChomozygous47524443
167410481574104816AG28GENIChomozygous47524445
167410503974105040TC19GENIChomozygous47697488
167410553774105538AAG12GENIChomozygous47524447
167411673674116737GA17GENIChomozygous47524449
167411689374116894GA20GENIChomozygous47697489
167411819774118198GA20GENIChomozygous47697490
167411904974119050TC16GENIChomozygous47697491
167411910374119104TC14GENIChomozygous47697492
167411925474119255CA23GENIChomozygous47697493
167411935974119360AG30GENIChomozygous47697494
167411950974119510CG26GENIChomozygous47697495
167412026974120270AT21GENIChomozygous47697496
167412053474120535AG17GENIChomozygous47697497
167412087074120871TC12GENIChomozygous47697498
167412092474120925CT6GENIChomozygous47697499
167412117974121180AG14GENIChomozygous47697500
167412128074121281AG23GENIChomozygous47524451
167412165474121655TA27GENICpossibly homozygous47697501
167412218174122182CT7GENIChomozygous47697504
167409964574099675TCAGAGAAATAGTTTCCTGTCTGGAGTATC------------------------------2INTERGENIChomozygous48142302
167410139574101424ACCCAAGCCTGTGGACATTTTGGGGAAGG-----------------------------1INTERGENIChomozygous48142304
167412173774121738TC16GENIChomozygous47697502
167412194874121949CT17GENIChomozygous47697503
167412218974122190GGAGAGCTTCATA7GENIChomozygous47697506
167412240874122409CCTTTTTTT5GENIChomozygous47945805
167412248674122487GA11GENIChomozygous47697507
167412253974122540AG15GENIChomozygous47697508
167412255474122555GA16GENIChomozygous47697509
167412256374122564TC17GENIChomozygous47697510
167412285274122856GGAG----14GENIChomozygous47697511