Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45517779-45517968 | Common:1; Rare:80 | ||||
chr19:45717264-45717532 | Common:1; Rare:86 | ||||
chr19:46860778-46861126 | Common:3; Rare:113 | ||||
chr19:47095154-47095172 | Rare:3 | ||||
chr19:47190263-47190437 | Common:1; Rare:30 | ||||
chr19:47503426-47503608 | Common:1; Rare:51 | ||||
chr19:48707368-48707716 | Common:5; Rare:49 | ||||
chr19:48962418-48962556 | Common:1; Rare:35 | ||||
chr19:48966275-48966730 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:49098436-49098675 | Rare:62 | ||||
chr19:49103570-49103793 | Common:1; Rare:72 | ||||
chr19:49103808-49103918 | Rare:38 | ||||
chr19:49133109-49133260 | Common:2; Rare:46 | ||||
chr19:49166716-49166744 | Rare:4 | ||||
chr19:49200306-49200665 | Common:3; Rare:144; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 |