| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142963327-142963675 | Common:1; Rare:94 | ||||
| chr3:142963976-142964078 | Common:2; Rare:26 | ||||
| chr3:143001445-143001625 | Common:3; Rare:63 | ||||
| chr3:148991421-148991645 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr3:149129549-149129676 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377494-149377837 | Common:1; Rare:93 | ||||
| chr3:149657953-149658175 | Rare:46 | ||||
| chr3:150408633-150408660 | Rare:9 | ||||
| chr3:150603139-150603365 | Common:2; Rare:87 | ||||
| chr3:150703187-150703528 | Rare:77 | ||||
| chr3:152268501-152269192 | Common:2; Rare:243 | ||||
| chr3:152269200-152269358 | Rare:45 | ||||
| chr3:152269509-152269749 | Common:2; Rare:71 | ||||
| chr3:154121315-154121451 | Common:2; Rare:62 | ||||
| chr3:154324413-154324573 | Rare:63 |