chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91778455217784553GA14GENIChomozygous117769185
91778457317784574AC12GENIChomozygous117676325
91778469117784692TC4GENIChomozygous117676327
91778474017784741CT8GENIChomozygous117676329
91778515617785157TC6GENIChomozygous117676331
91778516417785165TG7GENIChomozygous117676333
91778521817785219GA14GENIChomozygous117676335
91778534617785347TA16GENIChomozygous117676337
91778613917786140TG18GENIChomozygous117676339
91778638517786386AG14GENIChomozygous117676341
91778639117786392GA16GENIChomozygous117676343
91778645417786455TC16GENIChomozygous117676345
91778653117786532TC12GENIChomozygous117676347
91778697617786977TA11GENICpossibly homozygous117676349
91778723717787238GC16GENIChomozygous117676351
91778734917787350AG13GENIChomozygous117676353
91778742917787430GA16GENIChomozygous117676355
91778770817787709GT19GENIChomozygous117676357
91778800717788008CA15GENIChomozygous117676360
91778918817789189CT10GENIChomozygous117676362
91778930717789308CA10GENIChomozygous117676364
91779051217790513CT13GENIChomozygous117676366
91779764817797649TC13GENIChomozygous117676368
91778504417785045G11GENIChomozygous131064139
91778537917785381TT10GENIChomozygous131064140
91778619817786199T16GENIChomozygous131064141
91778625617786256AAC13GENIChomozygous131064142
91778626217786262ACAAACAAACAAAC13GENIChomozygous131064143
91778623617786236A13GENICheterozygous130377235