| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39782746-39783044 | Common:1; Rare:88 | ||||
| chr15:39920867-39921231 | Common:5; Rare:117 | ||||
| chr15:39933936-39934244 | Common:4; Rare:114 | ||||
| chr15:40039043-40039413 | Common:2; Rare:131 | ||||
| chr15:40105634-40105857 | Common:3; Rare:70 | ||||
| chr15:40106908-40106994 | Common:1; Rare:11 | ||||
| chr15:40108813-40109131 | Common:2; Rare:86 | ||||
| chr15:40160854-40161139 | Common:5; Rare:72 | ||||
| chr15:40307730-40308137 | Common:3; Rare:99 | ||||
| chr15:40308223-40308622 | Common:3; Rare:99 | ||||
| chr15:40382806-40383035 | Common:1; Rare:114 | ||||
| chr15:40383370-40383393 | Rare:6 | ||||
| chr15:40405554-40405881 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr15:40406251-40406329 | Rare:18 | ||||
| chr15:40440700-40441020 | Rare:89 |