| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40763788-40764146 | Common:3; Rare:89 | ||||
| chr15:40807050-40807125 | Rare:20 | ||||
| chr15:40807407-40807761 | Common:4; Rare:118 | ||||
| chr15:40843826-40844054 | Common:3; Rare:68 | ||||
| chr15:40844175-40844213 | Rare:13 | ||||
| chr15:40844216-40844495 | Rare:73 | ||||
| chr15:40894362-40894545 | Rare:50 | ||||
| chr15:40953199-40953479 | Common:2; Rare:75 | ||||
| chr15:41115982-41116061 | Rare:27 | ||||
| chr15:41116566-41116658 | Rare:29 | ||||
| chr15:41402427-41402558 | Common:4; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416976-41417296 | Common:3; Rare:121 | ||||
| chr15:41621453-41621552 | Common:1; Rare:23 | ||||
| chr15:41660321-41660535 | Rare:73 | ||||
| chr15:41972439-41972838 | Common:2; Rare:120 |