chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117460914117460915GT23GENIChomozygous947466358
8117462354117462355CT22GENIChomozygous947466359
8117463142117463143AG12GENIChomozygous947466360
8117463763117463764CT35GENIChomozygous947466361
8117464601117464602TC28GENIChomozygous947466362
8117464876117464877GA22GENIChomozygous947466363
8117466249117466250AC23GENIChomozygous947466364
8117466513117466514TC41GENIChomozygous947466365
8117467475117467476TG14GENIChomozygous947466366
8117467476117467477TG14GENIChomozygous947466367
8117468441117468442GA24GENIChomozygous947466368
8117469362117469363TC24GENIChomozygous947466369
8117470014117470015TC22GENIChomozygous947466370
8117471283117471284TC28GENIChomozygous947466371
8117471357117471358AT33GENIChomozygous947466372
8117473215117473216GA25GENICpossibly homozygous947466373
8117475110117475111CA22GENIChomozygous947466374