chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122264255622642557GT16GENIChomozygous115282424
122264256722642568GA13GENIChomozygous115282426
122264291222642913CT23GENIChomozygous115282428
122264301222643013GA24GENIChomozygous115282430
122264319122643192GA36GENIChomozygous115282432
122264401322644014AG20GENIChomozygous115282434
122264499422644995GT6GENIChomozygous115366953
122264524222645243GA13GENIChomozygous115282438
122264533222645333GA16GENICpossibly homozygous115282440
122264542422645425GA24GENIChomozygous115282442
122264548622645487CT13GENIChomozygous115282444
122264708922647090TC9GENIChomozygous115366955
122265123122651232CT29GENIChomozygous115282462
122265125922651260TG26GENIChomozygous115282464