chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117460914117460915GT27GENIChomozygous116671504
8117462354117462355CT24GENIChomozygous116671506
8117463142117463143AG13GENIChomozygous116671508
8117463763117463764CT22GENIChomozygous116671510
8117464369117464370AG2GENIChomozygous116671512
8117464395117464396CG6GENIChomozygous116671514
8117464601117464602TC19GENIChomozygous116671516
8117464876117464877GA21GENIChomozygous116671518
8117466249117466250AC24GENIChomozygous116671520
8117466513117466514TC29GENIChomozygous116671522
8117467475117467476TG5GENIChomozygous116671524
8117467476117467477TG5GENIChomozygous116671526
8117468441117468442GA20GENIChomozygous116671530
8117468564117468565GA14GENIChomozygous116671532
8117469362117469363TC29GENIChomozygous116671536
8117470014117470015TC18GENIChomozygous116671538
8117471283117471284TC30GENIChomozygous116671542
8117471357117471358AT24GENIChomozygous116671544
8117473215117473216GA25GENIChomozygous116671554
8117475110117475111CA29GENIChomozygous116671590