| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:37100987-37101529 | Common:25; Rare:150 | ||||
| chr15:37101682-37101864 | Common:1; Rare:59 | ||||
| chr15:38253562-38253791 | Common:3; Rare:53 | ||||
| chr15:38454025-38454227 | Rare:76 | ||||
| chr15:38454321-38454413 | Common:1; Rare:21 | ||||
| chr15:38454484-38454646 | Rare:49 | ||||
| chr15:39580765-39581159 | Common:2; Rare:106 | ||||
| chr15:39782428-39782694 | Common:2; Rare:72 | ||||
| chr15:39782763-39783003 | Common:1; Rare:74 | ||||
| chr15:39920051-39920379 | Common:1; Rare:58 | ||||
| chr15:39920734-39921138 | Common:4; Rare:129 | ||||
| chr15:39933655-39933755 | Common:1; Rare:26 | ||||
| chr15:39933853-39934278 | Common:4; Rare:135; Clinvar (benign):1 | ||||
| chr15:39934289-39934368 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr15:39934371-39934445 | Rare:10 |