chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31565922615659227CT30GENICpossibly homozygous136643510
31565984415659845GA14GENIChomozygous136643511
31566471115664712TG18GENIChomozygous136643512
31566479515664796AG21GENIChomozygous136643513
31566720715667208GA21GENIChomozygous136643514
31566731715667318CT21GENIChomozygous136643515
31566732715667328TC21GENIChomozygous136643516
31566743415667435CT17GENIChomozygous136643517
31566765815667659AG21GENIChomozygous136643518
31566787915667880AG13GENIChomozygous136643519
31566813615668137TC16GENIChomozygous136643520
31566860815668609CT21GENIChomozygous136643521
31566931215669313GA20GENIChomozygous136643522
31566942515669426TA22GENICpossibly homozygous136643523
31566998015669981GC19GENIChomozygous136643524
31567043315670434GA17GENIChomozygous136643525
31567152715671528TG12GENIChomozygous136643526
31567200415672005GA25GENIChomozygous136643527
31567268415672685AG22GENIChomozygous136643528
31567302615673027TG23GENIChomozygous136643529
31567325015673251AG19GENIChomozygous136643530
31567537815675379GA13GENIChomozygous136643531
31567442915674429AGGG27GENIChomozygous136549649
31566904915669080GGAGGCTGAGTACTAGTAATAGAGTTACGTT21GENIChomozygous136549647
31566942815669428TTC22GENICpossibly homozygous136549648