| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:36320580-36320766 | Common:3; Rare:60 | ||||
| chr14:37172569-37172591 | Rare:10 | ||||
| chr14:37197860-37198087 | Common:3; Rare:74 | ||||
| chr14:38208167-38208401 | Common:2; Rare:40 | ||||
| chr14:39114115-39114341 | Common:2; Rare:66 | ||||
| chr14:39175081-39175282 | Common:2; Rare:70 | ||||
| chr14:39267057-39267428 | Common:2; Rare:133 | ||||
| chr14:39432420-39432650 | Common:6; Rare:79 | ||||
| chr14:41608179-41608364 | Rare:44 | ||||
| chr14:44961892-44962267 | Common:3; Rare:109 | ||||
| chr14:45083989-45084174 | Rare:69 | ||||
| chr14:45135723-45135979 | Common:1; Rare:48 | ||||
| chr14:45253140-45253312 | Rare:43 | ||||
| chr14:49586316-49586770 | Common:1; Rare:239; Clinvar (benign):1 | ||||
| chr14:49598725-49599015 | Common:1; Rare:106 |