| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40340890-40341021 | Common:1; Rare:51 | ||||
| chr15:40382828-40383059 | Common:1; Rare:116 | ||||
| chr15:40405613-40405827 | Common:2; Rare:62; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569192-40569374 | Common:3; Rare:47 | ||||
| chr15:40593906-40594028 | Common:1; Rare:57 | ||||
| chr15:40694704-40694777 | Rare:16 | ||||
| chr15:40695050-40695236 | Common:2; Rare:57 | ||||
| chr15:40755212-40755375 | Common:1; Rare:55 | ||||
| chr15:40807027-40807119 | Rare:20 | ||||
| chr15:40807405-40807783 | Common:4; Rare:126 | ||||
| chr15:40894361-40894530 | Rare:49 | ||||
| chr15:40953181-40953488 | Common:2; Rare:84 | ||||
| chr15:41115981-41116097 | Rare:36 | ||||
| chr15:41116566-41116699 | Rare:41 | ||||
| chr15:41230755-41230870 | Rare:28 |