| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150603139-150603409 | Common:2; Rare:109 | ||||
| chr3:150703389-150703552 | Rare:45 | ||||
| chr3:151384729-151384978 | Common:1; Rare:42 | ||||
| chr3:152244261-152244392 | Common:1; Rare:19 | ||||
| chr3:152268439-152268677 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr3:152268829-152269179 | Rare:115 | ||||
| chr3:152269194-152269377 | Rare:53 | ||||
| chr3:152269529-152269772 | Common:2; Rare:68 | ||||
| chr3:152298720-152299080 | Rare:62 | ||||
| chr3:152834751-152834915 | Common:1; Rare:34 | ||||
| chr3:152834995-152835128 | Common:1; Rare:48 | ||||
| chr3:154121295-154121444 | Common:2; Rare:67 | ||||
| chr3:154324412-154324573 | Rare:63 | ||||
| chr3:155854364-155854815 | Rare:130 | ||||
| chr3:155870323-155870749 | Common:2; Rare:120 |