chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94536283945362840GA8GENICpossibly homozygous52618668
94536302845363029T-4GENIChomozygous52190099
94536338845363389TC15GENICpossibly homozygous52391223
94536408345364084CT23GENIChomozygous52618670
94536471445364715GA14GENIChomozygous52618672
94536517145365172CT22GENIChomozygous52618674
94536528045365281TC9GENIChomozygous52190101
94536528745365291TGTT----9GENIChomozygous52618676
94536364645363647AG19GENIChomozygous52391225
94536595545365956AG13GENIChomozygous52618678
94536810545368106GA14GENICpossibly homozygous52618680
94536813245368133GA16GENICpossibly homozygous52618682
94536815745368158GA20GENIChomozygous52190105