| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104800737-104800826 | Rare:18 | ||||
| chr14:104800900-104801047 | Common:1; Rare:39 | ||||
| chr14:104864723-104864903 | Rare:33 | ||||
| chr14:104865101-104865492 | Common:7; Rare:104 | ||||
| chr14:104865643-104866219 | Common:1; Rare:135 | ||||
| chr14:104970395-104970596 | Common:4; Rare:37 | ||||
| chr14:104970673-104970901 | Common:1; Rare:48 | ||||
| chr14:104978047-104978134 | Rare:23 | ||||
| chr14:104978279-104978478 | Common:1; Rare:65 | ||||
| chr14:104985580-104986033 | Common:6; Rare:165 | ||||
| chr14:104986143-104986351 | Common:2; Rare:43 | ||||
| chr14:104986394-104986426 | Rare:18 | ||||
| chr14:105020882-105021550 | Common:3; Rare:232 | ||||
| chr14:105168045-105168558 | Common:3; Rare:136; Clinvar (benign):1 | ||||
| chr14:105168675-105168933 | Rare:74 |