chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69549986195499862GA18GENIChomozygous137852664
69550022395500224AT23GENIChomozygous137852665
69550053695500536C16GENIChomozygous137698616
69550129795501298AG18GENIChomozygous137852666
69550231395502314AG17GENIChomozygous137852667
69550236395502364GA14GENIChomozygous137852668
69550426195504261C18GENIChomozygous137698617
69550461895504619AG27GENIChomozygous137852669
69550556895505569T17GENIChomozygous137698618
69550591695505917TG23GENIChomozygous137852670
69551000795510007ATTCAT7GENIChomozygous137698619
69551077195510772A14GENIChomozygous137698620
69551149595511496CT2GENIChomozygous141117032
69550698495506985GA16GENIChomozygous137852671
69551077495510775AC14GENIChomozygous137852672
69551193195511932T22GENIChomozygous137698621
69551203495512036AC16GENIChomozygous137698622
69551251495512515CT16GENIChomozygous137852673
69551268595512686A18GENIChomozygous137698623
69551396095513961GT20GENIChomozygous137852674
69551418695514187CT18GENIChomozygous137852675
69551483195514832GA15GENIChomozygous137852676
69551621195516212G12GENICpossibly homozygous137698624
69551645995516460GC20GENIChomozygous137852677
69551784995517850AG18GENIChomozygous137852678
69551921895519219CA13GENIChomozygous137852679
69551922895519229TC14GENIChomozygous137852680
69551930195519302TC14GENIChomozygous137852681
69551950495519505TC25GENIChomozygous137852682