| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54115613-54115797 | Common:2; Rare:47; Clinvar:5 | ||||
| chr19:54200658-54200898 | Common:3; Rare:92 | ||||
| chr19:54449039-54449220 | Common:2; Rare:48 | ||||
| chr19:55385731-55385961 | Common:5; Rare:79 | ||||
| chr19:55643523-55643649 | Rare:38 | ||||
| chr19:57279867-57279984 | Rare:32 | ||||
| chr19:57280305-57280502 | Common:1; Rare:64 | ||||
| chr19:57363251-57363584 | Common:4; Rare:108 | ||||
| chr19:57614133-57614267 | Common:3; Rare:51 | ||||
| chr19:57889002-57889188 | Common:1; Rare:58 | ||||
| chr19:58183311-58183431 | Rare:42 | ||||
| chr19:58278664-58278981 | Common:3; Rare:97 | ||||
| chr19:58326860-58327043 | Common:1; Rare:40 | ||||
| chr19:58347605-58347774 | Common:7; Rare:80 | ||||
| chr19:58499200-58499526 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):1 |