| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55993551-55993834 | Common:1; Rare:88 | ||||
| chr15:56918416-56918739 | Common:2; Rare:115 | ||||
| chr15:58749620-58750033 | Common:4; Rare:131 | ||||
| chr15:58771017-58771327 | Common:2; Rare:123 | ||||
| chr15:58933548-58933775 | Common:2; Rare:99 | ||||
| chr15:59372546-59372689 | Common:1; Rare:36 | ||||
| chr15:59372816-59372888 | Rare:30 | ||||
| chr15:59689230-59689572 | Common:9; Rare:165 | ||||
| chr15:60479060-60479213 | Common:2; Rare:65 | ||||
| chr15:62060358-62060511 | Rare:61 | ||||
| chr15:62165278-62165413 | Common:1; Rare:38 | ||||
| chr15:62390445-62390586 | Rare:66 | ||||
| chr15:62835387-62835757 | Common:2; Rare:101 | ||||
| chr15:63042658-63042943 | Rare:82; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:63157402-63157527 | Common:1; Rare:58 |