chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142108366142108367A16GENIChomozygous131025758
7142108595142108596TC17GENIChomozygous116097456
7142111295142111296AG12GENIChomozygous116097458
7142113026142113026A15GENICpossibly homozygous131025759
7142114193142114194CT20GENIChomozygous116097460
7142116047142116048CT20GENIChomozygous115941387
7142116249142116250TC21GENIChomozygous115941388
7142116258142116259CT20GENIChomozygous115941389
7142116946142116947AG13GENIChomozygous115941391
7142116993142116994TG13GENIChomozygous116097462
7142117444142117444A18GENICheterozygous131875198
7142117902142117903TC16GENIChomozygous116097464
7142117905142117909GTGT15GENIChomozygous131025760
7142117968142117969CT14GENIChomozygous122877561
7142117989142117995GTGCGC17GENIChomozygous131025761
7142118001142118002GA18GENIChomozygous122877563
7142118004142118005CT19GENIChomozygous116097470
7142118015142118019GTGC22GENIChomozygous131025762
7142118023142118025GC22GENIChomozygous131025763
7142118028142118029TC22GENIChomozygous122877566
7142119389142119390AG20GENIChomozygous115941394
7142119769142119770CG12GENIChomozygous115941396