| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42495508-42495713 | Common:2; Rare:63 | ||||
| chr15:42548733-42548875 | Common:1; Rare:83 | ||||
| chr15:43106015-43106231 | Rare:68 | ||||
| chr15:43330275-43330348 | Rare:39 | ||||
| chr15:43330564-43330734 | Common:1; Rare:62 | ||||
| chr15:43371030-43371180 | Common:1; Rare:34 | ||||
| chr15:43510676-43510954 | Rare:90 | ||||
| chr15:43517475-43517659 | Common:2; Rare:47 | ||||
| chr15:43746275-43746467 | Common:1; Rare:74 | ||||
| chr15:44288393-44288737 | Common:38; Rare:214 | ||||
| chr15:44536663-44537204 | Common:1; Rare:165 | ||||
| chr15:44711358-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711879-44711977 | Rare:21 | ||||
| chr15:45201119-45201135 | Common:1; Rare:9 | ||||
| chr15:45587083-45587470 | Common:1; Rare:93; Clinvar:6; Clinvar (benign):1 |