| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81436433-81436639 | Common:1; Rare:79 | ||||
| chr14:88562907-88563168 | Rare:113 | ||||
| chr14:88824350-88824716 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89416926-89417153 | Rare:70 | ||||
| chr14:89954693-89954884 | Rare:51 | ||||
| chr14:91510254-91510391 | Rare:47 | ||||
| chr14:91510447-91510637 | Common:1; Rare:59 | ||||
| chr14:91836421-91836688 | Common:12; Rare:46 | ||||
| chr14:92040019-92040192 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121667-92122000 | Common:4; Rare:111 | ||||
| chr14:92513300-92513421 | Common:2; Rare:27 | ||||
| chr14:92793995-92794408 | Rare:135 | ||||
| chr14:93184843-93185004 | Rare:52 | ||||
| chr14:93206989-93207288 | Common:2; Rare:146 | ||||
| chr14:94081125-94081406 | Common:5; Rare:86 |