| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43106018-43106175 | Rare:47 | ||||
| chr15:43330537-43330711 | Rare:66 | ||||
| chr15:43371036-43371127 | Rare:19 | ||||
| chr15:43510688-43510954 | Rare:85 | ||||
| chr15:43517438-43517653 | Common:2; Rare:47 | ||||
| chr15:43746275-43746704 | Common:2; Rare:172 | ||||
| chr15:43777114-43777405 | Rare:65 | ||||
| chr15:44536852-44537225 | Common:3; Rare:137 | ||||
| chr15:44663637-44663842 | Rare:86; Clinvar:2 | ||||
| chr15:44711355-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023052-45023248 | Common:3; Rare:53 | ||||
| chr15:45200496-45200656 | Common:1; Rare:44 | ||||
| chr15:45201108-45201133 | Common:1; Rare:13 | ||||
| chr15:45587110-45587265 | Rare:27 | ||||
| chr15:45587286-45587474 | Common:1; Rare:57; Clinvar:6; Clinvar (benign):1 |