| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40807411-40807791 | Common:4; Rare:129 | ||||
| chr15:40953253-40953475 | Common:1; Rare:62 | ||||
| chr15:41972466-41972775 | Common:1; Rare:90 | ||||
| chr15:42273036-42273272 | Common:1; Rare:98 | ||||
| chr15:42273391-42273551 | Rare:63 | ||||
| chr15:42457500-42457679 | Rare:34 | ||||
| chr15:42548733-42548888 | Common:1; Rare:89 | ||||
| chr15:43330539-43330737 | Common:1; Rare:73 | ||||
| chr15:43371030-43371101 | Rare:13 | ||||
| chr15:43746285-43746459 | Common:1; Rare:68 | ||||
| chr15:44536863-44537221 | Common:3; Rare:131 | ||||
| chr15:44711312-44711614 | Rare:91; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44729333-44729548 | Common:1; Rare:46 | ||||
| chr15:48120883-48121159 | Rare:73 | ||||
| chr15:48878015-48878457 | Rare:167 |