| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:35546139-35546252 | Common:1; Rare:40 | ||||
| chr15:37100500-37100775 | Common:1; Rare:92 | ||||
| chr15:39580853-39581086 | Common:1; Rare:61 | ||||
| chr15:39934026-39934202 | Common:3; Rare:62 | ||||
| chr15:40039091-40039350 | Rare:101 | ||||
| chr15:40405561-40405827 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40695069-40695227 | Common:2; Rare:47 | ||||
| chr15:40807425-40807767 | Common:4; Rare:115 | ||||
| chr15:40844322-40844647 | Rare:114 | ||||
| chr15:40894365-40894477 | Rare:40 | ||||
| chr15:41416989-41417193 | Common:2; Rare:89 | ||||
| chr15:41621109-41621248 | Common:1; Rare:36 | ||||
| chr15:41621410-41621548 | Common:1; Rare:31 | ||||
| chr15:41827917-41828151 | Common:4; Rare:87 | ||||
| chr15:42273050-42273253 | Common:1; Rare:84 |