chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185410862654108627CT13GENIChomozygous110355336
185410904354109044CT22GENIChomozygous110355339
185410945754109458GA19GENIChomozygous110355343
185411033254110333AT33GENIChomozygous110538661
185411052154110522AG21GENIChomozygous110654447
185411063454110635AG30GENIChomozygous110538665
185411071454110715AG24GENIChomozygous110538667
185411155954111560GA17GENICpossibly homozygous110654448
185411219254112193AG30GENIChomozygous110731848
185411274754112748TG15GENIChomozygous110538669
185411276354112764TC14GENIChomozygous110355347
185411297554112976AG19GENIChomozygous110355349
185411339454113395AG31GENIChomozygous110538671
185411348054113481TC22GENIChomozygous110538673
185411413454114135GA14GENIChomozygous110538675
185411617854116179CG15GENIChomozygous110355355
185411717454117175CT27GENIChomozygous110355357
185411730354117304TG18GENIChomozygous110355359
185411832054118321AG40GENIChomozygous110355361
185411848954118490CT16GENIChomozygous110654450
185411858854118589CT31GENIChomozygous110355363
185411880154118802GT21GENIChomozygous110355365
185411930854119309AG32GENIChomozygous110355367
185412005754120058AT13GENIChomozygous110355369
185412270554122706AG21GENIChomozygous110355371