chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69549986195499862GA13GENIChomozygous137852664
69550022395500224AT14GENIChomozygous137852665
69550053695500536C16GENIChomozygous137698616
69550129795501298AG13GENIChomozygous137852666
69550231395502314AG20GENIChomozygous137852667
69550236395502364GA18GENIChomozygous137852668
69550426195504261C27GENIChomozygous137698617
69550461895504619AG15GENIChomozygous137852669
69550556895505569T14GENIChomozygous137698618
69550591695505917TG10GENIChomozygous137852670
69550698495506985GA17GENIChomozygous137852671
69551000795510007ATTCAT8GENIChomozygous137698619
69551077195510772A19GENIChomozygous137698620
69551077495510775AC19GENIChomozygous137852672
69551111695511117GC12GENIChomozygous140890000
69551112595511126GC13GENIChomozygous140890001
69551113195511132GC13GENIChomozygous140890002
69551114095511141GC13GENIChomozygous140890003
69551114695511147GC14GENIChomozygous140890004
69551116195511162GC15GENIChomozygous140890005
69551116795511168CG14GENIChomozygous140890006
69551122795511228GC10GENIChomozygous140890007
69551123695511237CG8GENIChomozygous140890008
69551127595511276CG4GENIChomozygous140890009
69551149595511496CT1GENIChomozygous141117032
69551193195511932T16GENIChomozygous137698621
69551203495512036AC19GENIChomozygous137698622
69551251495512515CT8GENIChomozygous137852673
69551268595512686A31GENIChomozygous137698623
69551396095513961GT11GENIChomozygous137852674
69551418695514187CT25GENIChomozygous137852675
69551483195514832GA14GENIChomozygous137852676
69551621195516212G5GENIChomozygous137698624
69551645995516460GC17GENIChomozygous137852677
69551784995517850AG16GENIChomozygous137852678
69551921895519219CA13GENIChomozygous137852679
69551922895519229TC12GENIChomozygous137852680
69551930195519302TC17GENIChomozygous137852681
69551950495519505TC17GENIChomozygous137852682