| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:33158530-33158660 | Common:1; Rare:25 | ||||
| chr15:33581200-33581276 | Rare:24 | ||||
| chr15:35495118-35495408 | Rare:65 | ||||
| chr15:38072736-38073100 | Common:3; Rare:92 | ||||
| chr15:38073333-38073448 | Rare:20 | ||||
| chr15:38226023-38226096 | Common:1; Rare:9 | ||||
| chr15:38226880-38227115 | Common:1; Rare:37 | ||||
| chr15:38254676-38254799 | Common:2; Rare:26 | ||||
| chr15:39213442-39213817 | Common:2; Rare:80 | ||||
| chr15:39269434-39269705 | Common:2; Rare:53 | ||||
| chr15:40081688-40081921 | Common:1; Rare:52 | ||||
| chr15:41283757-41284018 | Common:2; Rare:68 | ||||
| chr15:41661878-41662046 | Common:1; Rare:45 | ||||
| chr15:42392565-42392883 | Common:2; Rare:89; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr15:43911489-43911875 | Common:2; Rare:72 |