| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40358088-40358324 | Common:6; Rare:100 | ||||
| chr15:40382806-40383035 | Common:1; Rare:114 | ||||
| chr15:40405620-40405861 | Common:2; Rare:75; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40569192-40569360 | Common:3; Rare:38 | ||||
| chr15:40695058-40695162 | Rare:30 | ||||
| chr15:40755212-40755378 | Common:1; Rare:57 | ||||
| chr15:40764008-40764092 | Rare:19 | ||||
| chr15:40807044-40807146 | Rare:31 | ||||
| chr15:40807436-40807760 | Common:4; Rare:107 | ||||
| chr15:40894224-40894519 | Rare:84 | ||||
| chr15:40953171-40953475 | Common:1; Rare:81 | ||||
| chr15:41116209-41116311 | Rare:28 | ||||
| chr15:41116455-41116704 | Common:1; Rare:75 | ||||
| chr15:41230754-41230831 | Rare:17 | ||||
| chr15:41231084-41231362 | Rare:93 |