| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40308436-40309250 | Common:9; Rare:273 | ||||
| chr15:40323290-40323696 | Common:10; Rare:261 | ||||
| chr15:40452330-40452780 | Common:3; Rare:79 | ||||
| chr15:40471639-40471931 | Rare:89; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:40471937-40472431 | Common:2; Rare:220; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):11 | ||||
| chr15:40506988-40507388 | Common:2; Rare:121 | ||||
| chr15:40511570-40512070 | Common:6; Rare:221 | ||||
| chr15:40541621-40542268 | Rare:121 | ||||
| chr15:40543100-40543440 | Common:2; Rare:67 | ||||
| chr15:40550260-40550910 | Rare:152 | ||||
| chr15:40553192-40553361 | Rare:22 | ||||
| chr15:40553736-40554400 | Common:8; Rare:214 | ||||
| chr15:40558110-40558540 | Common:5; Rare:93 | ||||
| chr15:40558880-40559280 | Rare:100 | ||||
| chr15:40692228-40692628 | Common:3; Rare:117 |