| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532455-50532648 | Common:3; Rare:55 | ||||
| chr14:50668019-50668092 | Rare:29 | ||||
| chr14:50668287-50668556 | Common:3; Rare:97 | ||||
| chr14:50821657-50821823 | Rare:33 | ||||
| chr14:50944370-50944550 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095071-51095303 | Common:4; Rare:91 | ||||
| chr14:51240075-51240380 | Common:1; Rare:124 | ||||
| chr14:51651370-51651383 | Rare:1 | ||||
| chr14:51651438-51651484 | Rare:21 | ||||
| chr14:51651613-51651990 | Common:4; Rare:105 | ||||
| chr14:51846932-51847214 | Common:2; Rare:53 | ||||
| chr14:51860336-51860781 | Rare:110 | ||||
| chr14:51989369-51989690 | Common:2; Rare:106 | ||||
| chr14:52003974-52004239 | Common:1; Rare:91 | ||||
| chr14:52069050-52069215 | Common:2; Rare:32 |