| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42273373-42273633 | Common:1; Rare:94 | ||||
| chr15:42490993-42491252 | Common:1; Rare:74 | ||||
| chr15:42548448-42548491 | Common:1; Rare:13 | ||||
| chr15:42548702-42548875 | Common:2; Rare:92 | ||||
| chr15:42737112-42737265 | Common:1; Rare:59; Clinvar:1 | ||||
| chr15:43185379-43185492 | Rare:28 | ||||
| chr15:43330525-43330772 | Common:1; Rare:82 | ||||
| chr15:43371030-43371251 | Common:1; Rare:44 | ||||
| chr15:43510731-43511102 | Rare:142 | ||||
| chr15:43746285-43746704 | Common:2; Rare:169 | ||||
| chr15:44536647-44536692 | Rare:8 | ||||
| chr15:44536855-44537401 | Common:3; Rare:200 | ||||
| chr15:44663556-44663816 | Rare:133; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711314-44711611 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023048-45023241 | Common:3; Rare:51 |