| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001227-143001661 | Common:5; Rare:127 | ||||
| chr3:143971727-143972074 | Common:2; Rare:134 | ||||
| chr3:146160904-146161293 | Common:1; Rare:133; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146250802-146250855 | Common:1; Rare:12 | ||||
| chr3:146250967-146251200 | Common:1; Rare:54 | ||||
| chr3:146469288-146469477 | Common:4; Rare:37 | ||||
| chr3:146469551-146469625 | Rare:15 | ||||
| chr3:146544467-146544792 | Common:4; Rare:80 | ||||
| chr3:148991429-148991642 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr3:149086295-149086413 | Rare:33 | ||||
| chr3:149086418-149086731 | Rare:94 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377624-149377790 | Common:1; Rare:41 | ||||
| chr3:149657953-149658175 | Rare:46 | ||||
| chr3:149752406-149752579 | Common:2; Rare:62 |