| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34462182-34462558 | Common:1; Rare:138 | ||||
| chr14:34539553-34539888 | Common:1; Rare:97 | ||||
| chr14:34629944-34630252 | Common:5; Rare:123 | ||||
| chr14:34714538-34714734 | Common:2; Rare:72 | ||||
| chr14:34874806-34875025 | Common:2; Rare:69 | ||||
| chr14:34875136-34875465 | Rare:124 | ||||
| chr14:34982366-34982709 | Common:1; Rare:139 | ||||
| chr14:35046130-35046702 | Common:2; Rare:203 | ||||
| chr14:35121764-35121860 | Rare:25 | ||||
| chr14:35122173-35122355 | Rare:43 | ||||
| chr14:35122433-35122642 | Common:1; Rare:69 | ||||
| chr14:35122652-35122814 | Common:1; Rare:40 | ||||
| chr14:35292224-35292576 | Common:4; Rare:111; Clinvar:1 | ||||
| chr14:35404591-35404804 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:35826203-35826512 | Common:1; Rare:89 |