chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145961094459610945GC17GENIChomozygous48740786
145961107259611073CCTGTTTGTT10GENICpossibly homozygous49310627
145961137659611378AG--6GENIChomozygous48740792
145961255459612555GGCACACACACACACACACA1GENIChomozygous49310628
145961874759618748TC21GENIChomozygous48740796