chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117460914117460915GT23GENIChomozygous116671504
8117462354117462355CT22GENIChomozygous116671506
8117463142117463143AG12GENIChomozygous116671508
8117463763117463764CT35GENIChomozygous116671510
8117464601117464602TC28GENIChomozygous116671516
8117464876117464877GA22GENIChomozygous116671518
8117466249117466250AC23GENIChomozygous116671520
8117466513117466514TC41GENIChomozygous116671522
8117467475117467476TG14GENIChomozygous116671524
8117467476117467477TG14GENIChomozygous116671526
8117468441117468442GA24GENIChomozygous116671530
8117469362117469363TC24GENIChomozygous116671536
8117470014117470015TC22GENIChomozygous116671538
8117471283117471284TC28GENIChomozygous116671542
8117471357117471358AT33GENIChomozygous116671544
8117473215117473216GA25GENICpossibly homozygous116671554
8117475110117475111CA22GENIChomozygous116671590