| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143119645-143119914 | Common:1; Rare:85 | ||||
| chr3:146160949-146161271 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:148991436-148991632 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr3:149129549-149129701 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377531-149377841 | Common:1; Rare:80 | ||||
| chr3:149657974-149658189 | Rare:47 | ||||
| chr3:149813003-149813265 | Common:2; Rare:86 | ||||
| chr3:150603168-150603360 | Common:2; Rare:76 | ||||
| chr3:152268755-152269045 | Rare:109 | ||||
| chr3:152269533-152269689 | Rare:41 | ||||
| chr3:154121309-154121440 | Common:2; Rare:59 | ||||
| chr3:155079837-155080124 | Common:1; Rare:63 | ||||
| chr3:155854371-155854729 | Rare:101 | ||||
| chr3:156674374-156674635 | Common:3; Rare:73 | ||||
| chr3:157160065-157160324 | Rare:109 |