chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145961107259611073CCTGTTTGTT10GENICpossibly homozygous49310627
145961137659611378AG--17GENIChomozygous48740792
145961255459612555GGCACACACACACACACACA3GENICheterozygous49310628
145961255459612555GGCACACACACACACACA3GENICheterozygous49331485
145961874759618748TC22GENIChomozygous48740796
145962122459621225AG28GENIChomozygous48740798