| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146160967-146161389 | Common:4; Rare:248; Clinvar:10; Clinvar (benign):4 | ||||
| chr3:146161393-146161510 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:146222270-146222645 | Common:8; Rare:133 | ||||
| chr3:146251043-146251198 | Common:1; Rare:40 | ||||
| chr3:146544496-146544983 | Common:8; Rare:181 | ||||
| chr3:148991414-148991620 | Common:4; Rare:172; Clinvar (benign):2 | ||||
| chr3:149086453-149086738 | Rare:84 | ||||
| chr3:149129539-149129765 | Common:2; Rare:165; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:149377506-149377872 | Common:2; Rare:170 | ||||
| chr3:149657807-149658368 | Common:1; Rare:186 | ||||
| chr3:149670881-149671185 | Common:1; Rare:53 | ||||
| chr3:149812603-149812767 | Common:1; Rare:44 | ||||
| chr3:149813064-149813308 | Common:2; Rare:165 | ||||
| chr3:149969918-149970682 | Rare:297 | ||||
| chr3:149970730-149971347 | Common:10; Rare:419 |