| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:27608854-27609149 | Common:9; Rare:65 | ||||
| chr15:27621337-27621484 | Common:2; Rare:27 | ||||
| chr15:27655974-27656226 | Common:2; Rare:64 | ||||
| chr15:27713880-27714129 | Common:1; Rare:55 | ||||
| chr15:28027187-28027311 | Rare:45 | ||||
| chr15:28589192-28589521 | Common:1; Rare:10 | ||||
| chr15:28814006-28814061 | Rare:10 | ||||
| chr15:28832190-28832405 | Common:4; Rare:68 | ||||
| chr15:28848599-28848925 | Common:4; Rare:88 | ||||
| chr15:29207445-29207709 | Common:4; Rare:62 | ||||
| chr15:29224393-29224561 | Common:2; Rare:50 | ||||
| chr15:29268878-29269199 | Common:2; Rare:107; Clinvar (pathogenic):2 | ||||
| chr15:29686581-29686774 | Common:4; Rare:48 | ||||
| chr15:29730427-29730611 | Rare:41 | ||||
| chr15:30044535-30044624 | Common:2; Rare:21 |