| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43370821-43371192 | Common:4; Rare:85 | ||||
| chr15:43648854-43649025 | Common:2; Rare:60 | ||||
| chr15:43746285-43746459 | Common:1; Rare:68 | ||||
| chr15:43746529-43746704 | Common:1; Rare:63 | ||||
| chr15:43776961-43777071 | Rare:27 | ||||
| chr15:43777116-43777386 | Rare:64 | ||||
| chr15:44288367-44288785 | Common:39; Rare:231 | ||||
| chr15:44536663-44537227 | Common:3; Rare:180 | ||||
| chr15:44711321-44711612 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711673-44711982 | Rare:54 | ||||
| chr15:45378487-45378645 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr15:45587166-45587250 | Rare:15 | ||||
| chr15:45587297-45587461 | Rare:50; Clinvar:6 | ||||
| chr15:45634923-45635103 | Rare:53 | ||||
| chr15:48331383-48331465 | Rare:27 |