| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34583593-34583728 | Common:2; Rare:45 | ||||
| chr15:34988209-34988404 | Common:1; Rare:82 | ||||
| chr15:35546118-35546231 | Rare:43 | ||||
| chr15:36579529-36579733 | Common:2; Rare:57 | ||||
| chr15:37101200-37101231 | Rare:11 | ||||
| chr15:37101301-37101321 | Rare:3 | ||||
| chr15:38454072-38454197 | Rare:52 | ||||
| chr15:39782802-39782877 | Rare:20 | ||||
| chr15:39934045-39934187 | Common:3; Rare:52 | ||||
| chr15:40039081-40039335 | Rare:103 | ||||
| chr15:40160902-40161144 | Common:3; Rare:56 | ||||
| chr15:40405632-40405827 | Common:2; Rare:58; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40564987-40565216 | Common:3; Rare:41 | ||||
| chr15:40569192-40569346 | Common:3; Rare:30 | ||||
| chr15:40593901-40594035 | Common:1; Rare:63 |