| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232820-24232951 | Common:1; Rare:26 | ||||
| chr14:24290888-24291190 | Common:2; Rare:97 | ||||
| chr14:24299730-24299893 | Common:4; Rare:53 | ||||
| chr14:24429855-24430087 | Common:1; Rare:47 | ||||
| chr14:24442801-24443046 | Common:4; Rare:62 | ||||
| chr14:31207689-31207869 | Common:1; Rare:61 | ||||
| chr14:31420502-31420741 | Common:4; Rare:79 | ||||
| chr14:31561328-31561503 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076825-32077043 | Common:3; Rare:79 | ||||
| chr14:34462226-34462559 | Common:1; Rare:113 | ||||
| chr14:34982474-34982682 | Common:1; Rare:91 | ||||
| chr14:35046130-35046497 | Common:1; Rare:127 | ||||
| chr14:35046622-35046703 | Common:1; Rare:33 | ||||
| chr14:35121925-35122349 | Common:2; Rare:116 | ||||
| chr14:35122506-35122781 | Common:2; Rare:83 |