| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44862093-44862261 | Common:3; Rare:47 | ||||
| chr3:44975130-44975311 | Rare:26 | ||||
| chr3:44976066-44976280 | Common:2; Rare:85 | ||||
| chr3:45388378-45388653 | Common:2; Rare:75 | ||||
| chr3:45689180-45689474 | Common:1; Rare:98 | ||||
| chr3:45841976-45842299 | Common:3; Rare:94 | ||||
| chr3:45995776-45995961 | Common:2; Rare:39; Clinvar:1 | ||||
| chr3:46407054-46407271 | Rare:39 | ||||
| chr3:46693667-46693781 | Common:1; Rare:28 | ||||
| chr3:46863260-46863721 | Common:3; Rare:110; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr3:46882106-46882264 | Common:1; Rare:47 | ||||
| chr3:46979555-46979837 | Common:1; Rare:61; Clinvar:1 | ||||
| chr3:47163905-47164414 | Common:1; Rare:135 | ||||
| chr3:47380790-47381072 | Rare:89 | ||||
| chr3:47475791-47476069 | Common:3; Rare:111 |