| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40039091-40039329 | Rare:99 | ||||
| chr15:40382833-40382995 | Common:1; Rare:84 | ||||
| chr15:40807436-40807760 | Common:4; Rare:107 | ||||
| chr15:41416889-41417182 | Common:4; Rare:118 | ||||
| chr15:42208275-42208401 | Rare:41 | ||||
| chr15:42273416-42273516 | Rare:35 | ||||
| chr15:42491078-42491252 | Rare:45 | ||||
| chr15:42548719-42548870 | Common:2; Rare:82 | ||||
| chr15:43330586-43330674 | Rare:31 | ||||
| chr15:43371054-43371104 | Rare:10 | ||||
| chr15:43493101-43493350 | Common:1; Rare:76 | ||||
| chr15:43746287-43746464 | Common:1; Rare:68 | ||||
| chr15:44536862-44537191 | Common:1; Rare:116 | ||||
| chr15:44711336-44711608 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45587084-45587464 | Common:1; Rare:91; Clinvar:6; Clinvar (benign):1 |