chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142108366142108367A54GENIChomozygous131025758
7142108595142108596TC56GENIChomozygous116097456
7142111295142111296AG37GENIChomozygous116097458
7142113026142113026A49GENICpossibly homozygous131025759
7142114193142114194CT52GENIChomozygous116097460
7142116047142116048CT47GENIChomozygous115941387
7142116249142116250TC57GENIChomozygous115941388
7142116258142116259CT61GENIChomozygous115941389
7142116946142116947AG40GENIChomozygous115941391
7142117905142117909GTGT50GENIChomozygous131025760
7142117968142117969CT46GENIChomozygous122877561
7142117989142117995GTGCGC44GENIChomozygous131025761
7142118001142118002GA43GENIChomozygous122877563
7142118004142118005CT43GENIChomozygous116097470
7142118015142118019GTGC43GENIChomozygous131025762
7142118023142118025GC46GENIChomozygous131025763
7142118028142118029TC50GENIChomozygous122877566
7142119389142119390AG53GENIChomozygous115941394
7142119769142119770CG53GENICpossibly homozygous115941396
7142117867142117879GTGCGTGTGCGC45GENIChomozygous128530286
7142117941142117951GTGCGTGTGT51GENIChomozygous131435253