chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69549986195499862GA61GENIChomozygous137852664
69550022395500224AT58GENIChomozygous137852665
69550053695500536C56GENIChomozygous137698616
69550129795501298AG56GENIChomozygous137852666
69550231395502314AG60GENIChomozygous137852667
69550236395502364GA56GENICpossibly homozygous137852668
69550426195504261C53GENIChomozygous137698617
69550461895504619AG37GENIChomozygous137852669
69550556895505569T67GENIChomozygous137698618
69550591695505917TG69GENIChomozygous137852670
69550698495506985GA50GENIChomozygous137852671
69551077195510772A53GENIChomozygous137698620
69551077495510775AC53GENIChomozygous137852672
69551193195511932T59GENICpossibly homozygous137698621
69551203495512036AC57GENIChomozygous137698622
69551251495512515CT64GENIChomozygous137852673
69551268595512686A50GENIChomozygous137698623
69551396095513961GT40GENIChomozygous137852674
69551418695514187CT49GENIChomozygous137852675
69551483195514832GA53GENIChomozygous137852676
69551621195516212G21GENIChomozygous137698624
69551645995516460GC50GENIChomozygous137852677
69551784995517850AG60GENIChomozygous137852678
69551921895519219CA67GENIChomozygous137852679
69551922895519229TC65GENIChomozygous137852680
69551930195519302TC59GENIChomozygous137852681
69551950495519505TC49GENIChomozygous137852682