chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48124437981244384CGCGT26GENIChomozygous128054368
48124442481244424T26GENIChomozygous128054369
48124443281244433T30GENIChomozygous128054370
48124443581244436TC32GENIChomozygous119278547
48124516681245167A57GENICpossibly homozygous128054371
48124565881245658T59GENIChomozygous128054372
48124581281245813GA60GENIChomozygous112748299
48124720881247209AG57GENIChomozygous112748301
48124760481247604A56GENIChomozygous128054373
48125206781252068T54GENIChomozygous128054374
48125681081256824ATTTATATATATAT37GENICheterozygous130933286