chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91778455217784553GA21GENIChomozygous117769185
91778457317784574AC22GENIChomozygous117676325
91778469117784692TC21GENIChomozygous117676327
91778474017784741CT22GENIChomozygous117676329
91778515617785157TC20GENIChomozygous117676331
91778516417785165TG19GENIChomozygous117676333
91778521817785219GA19GENIChomozygous117676335
91778534617785347TA14GENIChomozygous117676337
91778613917786140TG19GENIChomozygous117676339
91778638517786386AG32GENIChomozygous117676341
91778639117786392GA33GENIChomozygous117676343
91778645417786455TC26GENIChomozygous117676345
91778653117786532TC19GENIChomozygous117676347
91778697617786977TA22GENIChomozygous117676349
91778723717787238GC20GENIChomozygous117676351
91778734917787350AG26GENIChomozygous117676353
91778742917787430GA21GENIChomozygous117676355
91778770817787709GT25GENICpossibly homozygous117676357
91778800717788008CA17GENIChomozygous117676360
91778918817789189CT26GENIChomozygous117676362
91778930717789308CA20GENIChomozygous117676364
91779051217790513CT30GENIChomozygous117676366
91778504417785045G19GENIChomozygous131064139
91778537917785381TT13GENIChomozygous131064140
91778619817786199T21GENIChomozygous131064141
91778625617786256AAC23GENIChomozygous131064142
91778626217786262ACAAACAAACAAAC24GENIChomozygous131064143
91778623617786236A19GENICheterozygous130377235
91779764817797649TC8GENIChomozygous117676368