chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145961094459610945GC17GENIChomozygous48740786
145961107259611073CCTGTT12GENICpossibly homozygous49405345
145961137659611378AG--16GENIChomozygous48740792
145961255459612555GGCACACACACACACACA1GENIChomozygous49331485
145961874759618748TC20GENIChomozygous48740796