chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2843707728437078CT17GENIChomozygous883926736
X2843822728438228CA3GENICheterozygous883926737
X2844104728441048GA5GENIChomozygous883926738
X2844527328445274CT11GENIChomozygous883926739
X2844935428449355TG22GENIChomozygous883926740
X2844959728449598AT9GENIChomozygous883926741
X2845039428450395AG13GENIChomozygous883926742
X2845082028450821CT10GENIChomozygous883926743
X2845083028450831TC10GENIChomozygous883926744
X2845218628452187CT16GENIChomozygous883926745
X2845221628452217GA21GENIChomozygous883926746
X2845245328452454TC17GENIChomozygous883926747
X2845256128452562GA19GENIChomozygous883926748
X2845304328453044GC12GENIChomozygous883926749
X2845305328453054CG17GENIChomozygous883926750
X2845428428454285GT19GENIChomozygous883926751
X2845431028454311TC20GENIChomozygous883926752
X2845460628454607AT24GENIChomozygous883926753
X2845545128455452TC17GENIChomozygous883926754
X2845583628455837CT15GENIChomozygous883926755
X2845671028456711GA12GENIChomozygous883926756
X2845672228456723CT17GENIChomozygous883926757
X2845676728456768TC16GENIChomozygous883926758
X2845727828457279AC17GENIChomozygous883926759
X2845771428457715GC18GENIChomozygous883926760
X2845990928459910CT27GENIChomozygous883926761
X2846012728460128GT16GENIChomozygous883926762
X2846053228460533GA14GENIChomozygous883926763
X2846108528461086AG21GENIChomozygous883926764
X2846294228462943GA20GENIChomozygous883926765
X2846351728463518CT21GENIChomozygous883926766
X2846437628464377CT12GENIChomozygous883926767
X2846453428464535GA15GENIChomozygous883926768
X2846522528465226TC26GENIChomozygous883926769
X2846556028465561AG17GENIChomozygous883926770
X2846556528465566AG22GENIChomozygous883926771
X2846832128468322TG8GENIChomozygous883926774