chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113171991631719917CT28GENIChomozygous799834409
113172086931720870AG28GENIChomozygous799834410
113172127731721278GA34GENIChomozygous799834411
113172270531722706TA26GENIChomozygous799834412
113172301131723012CT36GENIChomozygous799834413
113172385431723855GA35GENIChomozygous799834414
113172416031724161CG25GENIChomozygous799834415
113172470331724704AC33GENIChomozygous799834416
113172824931728250CA24GENIChomozygous799834417
113173103631731037CT33GENIChomozygous799834418
113173175931731760AG41GENICheterozygous799834419
113173176331731764AG41GENICheterozygous799834420
113173257431732575CT30GENIChomozygous799834421
113173276931732770TC32GENIChomozygous799834422
113173279931732800AG35GENIChomozygous799834423
113173446031734461AG30GENIChomozygous799834424
113173630931736310GA50GENIChomozygous799834425
113173680031736801TC31GENIChomozygous799834426
113173794831737949AG39GENICpossibly homozygous799834427
113173857731738578CT29GENIChomozygous799834428
113174003131740032TC55GENICheterozygous799834429
113174057731740578GA30GENIChomozygous799834430
113174185231741853GA40GENIChomozygous799834431
113174269531742696TC27GENICpossibly homozygous799834432
113174362231743623AT32GENIChomozygous799834433
113174391731743918GA31GENIChomozygous799834434
113174552431745525CT22GENIChomozygous799834435
113174664231746643CG27GENIChomozygous799834436
113174740931747410AT33GENICpossibly homozygous799834437
113174928231749283AT36GENIChomozygous799834438
113174963131749632GA40GENIChomozygous799834439
113174984131749842TC41GENIChomozygous799834440
113175017931750180GA28GENIChomozygous799834441
113175072231750723AG38GENIChomozygous799834442