| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40291119-40291178 | Rare:24 | ||||
| chr15:40291291-40291515 | Common:2; Rare:75 | ||||
| chr15:40338992-40339192 | Rare:51 | ||||
| chr15:40340288-40340340 | Rare:8 | ||||
| chr15:40340472-40340560 | Common:1; Rare:14 | ||||
| chr15:40340856-40341032 | Common:3; Rare:61 | ||||
| chr15:40382806-40383055 | Common:1; Rare:125 | ||||
| chr15:40383337-40383396 | Rare:18 | ||||
| chr15:40405534-40405692 | Rare:38; Clinvar:1 | ||||
| chr15:40405765-40405876 | Common:1; Rare:46; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr15:40406144-40406214 | Rare:15 | ||||
| chr15:40440052-40440127 | Rare:18 | ||||
| chr15:40440706-40441242 | Rare:177 | ||||
| chr15:40441249-40441446 | Common:1; Rare:56 | ||||
| chr15:40441557-40441731 | Rare:51 |