| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:37101244-37101485 | Common:25; Rare:89 | ||||
| chr15:37101690-37101925 | Common:2; Rare:78 | ||||
| chr15:38454072-38454194 | Rare:51 | ||||
| chr15:39782797-39782919 | Rare:34 | ||||
| chr15:39920910-39921088 | Common:2; Rare:63 | ||||
| chr15:39933998-39934220 | Common:4; Rare:82 | ||||
| chr15:40039076-40039367 | Common:1; Rare:109 | ||||
| chr15:40160918-40161146 | Common:3; Rare:53 | ||||
| chr15:40340917-40341005 | Common:1; Rare:33 | ||||
| chr15:40382814-40383043 | Common:1; Rare:112 | ||||
| chr15:40405582-40405827 | Common:2; Rare:69; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40564987-40565237 | Common:3; Rare:46 | ||||
| chr15:40569192-40569387 | Common:3; Rare:53 | ||||
| chr15:40593906-40594035 | Common:1; Rare:58 | ||||
| chr15:40594210-40594349 | Rare:34 |