chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4121348888121348889TG15GENIChomozygous143153558
4121349084121349085AG22GENIChomozygous143153559
4121349990121349990G23GENIChomozygous143061527
4121352193121352194A14GENIChomozygous143061528
4121353154121353155TC22GENIChomozygous143153563
4121350415121350416TC22GENIChomozygous143153560
4121351696121351697GA18GENIChomozygous143153561
4121352852121352853CT23GENIChomozygous143153562
4121353295121353296GA20GENIChomozygous143153564
4121353394121353395TC21GENIChomozygous143153565
4121353615121353616CA25GENIChomozygous143153566
4121356350121356350TT20GENIChomozygous143061529
4121358777121358778TC20GENIChomozygous143153567
4121358781121358782CA17GENIChomozygous143153568
4121358924121358925CT18GENIChomozygous143153569
4121359116121359117CT22GENIChomozygous143153570
4121359592121359593CA20GENIChomozygous143153571
4121359593121359594CT20GENIChomozygous143153572
4121359776121359777GA15GENIChomozygous143153573
4121360112121360113CT14GENIChomozygous143153574
4121360677121360678AG15GENICpossibly homozygous143153575
4121360846121360847GC17GENIChomozygous143153576