| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39920906-39921024 | Common:2; Rare:41 | ||||
| chr15:39934040-39934220 | Common:3; Rare:71 | ||||
| chr15:40038860-40039356 | Common:2; Rare:174 | ||||
| chr15:40106589-40106759 | Rare:27 | ||||
| chr15:40252309-40252681 | Common:3; Rare:137 | ||||
| chr15:40307834-40308041 | Common:1; Rare:49 | ||||
| chr15:40340203-40340369 | Rare:30 | ||||
| chr15:40340815-40341040 | Common:4; Rare:81 | ||||
| chr15:40358143-40358328 | Common:5; Rare:80 | ||||
| chr15:40382806-40383049 | Common:1; Rare:121 | ||||
| chr15:40405562-40405612 | Rare:11; Clinvar:1 | ||||
| chr15:40405620-40405983 | Common:2; Rare:117; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr15:40406293-40406544 | Rare:43 | ||||
| chr15:40407780-40407999 | Common:4; Rare:61; Clinvar (benign):3 | ||||
| chr15:40695034-40695180 | Rare:43 |