| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142225583-142225646 | Rare:14 | ||||
| chr3:142447974-142448122 | Common:1; Rare:51 | ||||
| chr3:142578729-142578948 | Rare:71; Clinvar:1 | ||||
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:149086452-149086656 | Rare:57 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149812647-149812745 | Common:1; Rare:29 | ||||
| chr3:149813045-149813274 | Common:1; Rare:79 | ||||
| chr3:150603134-150603409 | Common:2; Rare:110 | ||||
| chr3:150703910-150704013 | Rare:36 | ||||
| chr3:152268568-152269053 | Common:2; Rare:181 | ||||
| chr3:152269549-152269678 | Rare:34 | ||||
| chr3:154324430-154324573 | Rare:51 | ||||
| chr3:155079577-155079706 | Common:5; Rare:39 | ||||
| chr3:155079823-155079905 | Common:1; Rare:26 |