| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42208236-42208401 | Rare:52 | ||||
| chr15:42273054-42273272 | Common:1; Rare:94 | ||||
| chr15:42273394-42273666 | Rare:97 | ||||
| chr15:42491002-42491196 | Common:1; Rare:63 | ||||
| chr15:42495508-42495705 | Common:2; Rare:58 | ||||
| chr15:42548422-42548882 | Common:5; Rare:165 | ||||
| chr15:43106028-43106175 | Rare:44 | ||||
| chr15:43330019-43330337 | Common:2; Rare:165 | ||||
| chr15:43330543-43330737 | Common:1; Rare:72 | ||||
| chr15:43370989-43371131 | Rare:38 | ||||
| chr15:43510669-43510954 | Rare:91 | ||||
| chr15:43746275-43746446 | Common:1; Rare:65 | ||||
| chr15:43824603-43824818 | Common:2; Rare:58 | ||||
| chr15:44536863-44537227 | Common:3; Rare:136 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 |