| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24036793-24036923 | Common:2; Rare:37 | ||||
| chr14:24066645-24066887 | Rare:42 | ||||
| chr14:24081101-24081320 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:24140742-24140920 | Rare:55 | ||||
| chr14:24243318-24243419 | Common:1; Rare:20 | ||||
| chr14:24243498-24243558 | Rare:6 | ||||
| chr14:24252573-24252675 | Common:1; Rare:15 | ||||
| chr14:24316332-24316398 | Rare:23 | ||||
| chr14:24427033-24427132 | Common:1; Rare:14 | ||||
| chr14:24818163-24818453 | Common:3; Rare:53 | ||||
| chr14:24839054-24839117 | Common:1; Rare:13 | ||||
| chr14:24861115-24861231 | Rare:22 | ||||
| chr14:24885453-24885650 | Common:1; Rare:44 | ||||
| chr14:24979190-24979353 | Common:1; Rare:29 | ||||
| chr14:25001086-25001296 | Common:1; Rare:29 |