| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001472-143001634 | Common:2; Rare:57 | ||||
| chr3:146161015-146161131 | Rare:48; Clinvar:3 | ||||
| chr3:149970872-149971027 | Rare:86 | ||||
| chr3:150408169-150408367 | Common:2; Rare:84 | ||||
| chr3:150603162-150603305 | Common:1; Rare:46 | ||||
| chr3:152268574-152268953 | Common:2; Rare:147 | ||||
| chr3:152269551-152269669 | Rare:33 | ||||
| chr3:156674350-156674614 | Common:3; Rare:78 | ||||
| chr3:157160139-157160288 | Rare:61 | ||||
| chr3:160399185-160399307 | Rare:33; Clinvar:2 | ||||
| chr3:160399495-160399718 | Rare:66; Clinvar:1 | ||||
| chr3:160565394-160565868 | Common:2; Rare:167 | ||||
| chr3:167734832-167735202 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735573-167735758 | Rare:47 | ||||
| chr3:169773314-169773426 | Rare:38 |