| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129495-149129711 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377610-149377812 | Common:1; Rare:50 | ||||
| chr3:149752299-149752603 | Common:2; Rare:116 | ||||
| chr3:149813087-149813265 | Common:1; Rare:63 | ||||
| chr3:150408090-150408306 | Common:1; Rare:74 | ||||
| chr3:150408736-150408988 | Rare:79 | ||||
| chr3:150603139-150603389 | Common:2; Rare:97 | ||||
| chr3:152268646-152268978 | Rare:133 | ||||
| chr3:152269529-152269691 | Rare:46 | ||||
| chr3:154121290-154121457 | Common:3; Rare:75 | ||||
| chr3:154324412-154324646 | Rare:82 | ||||
| chr3:155854364-155854748 | Rare:107 | ||||
| chr3:156555081-156555419 | Common:2; Rare:119 | ||||
| chr3:156674373-156674618 | Common:3; Rare:67 | ||||
| chr3:157160072-157160315 | Rare:103 |