| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10309905-10309945 | Rare:6 | ||||
| chr3:10310058-10310149 | Common:1; Rare:17 | ||||
| chr3:10311044-10311488 | Common:4; Rare:79 | ||||
| chr3:11351639-11351832 | Common:1; Rare:24 | ||||
| chr3:11362715-11362856 | Rare:28 | ||||
| chr3:11600457-11600641 | Common:1; Rare:28 | ||||
| chr3:11641742-11641815 | Rare:17 | ||||
| chr3:11804320-11804588 | Rare:44 | ||||
| chr3:12584925-12585149 | Common:1; Rare:74; Clinvar:10; Clinvar (benign):8 | ||||
| chr3:12587514-12587935 | Common:1; Rare:79 | ||||
| chr3:12662738-12662971 | Common:1; Rare:56 | ||||
| chr3:14128481-14128564 | Common:1; Rare:15 | ||||
| chr3:14128574-14128802 | Common:1; Rare:45 | ||||
| chr3:14130511-14130939 | Common:3; Rare:135; Clinvar:8; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr3:14155099-14155421 | Common:1; Rare:56 |