| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55318893-55319420 | Common:4; Rare:156 | ||||
| chr15:55319447-55319483 | Rare:7 | ||||
| chr15:55407992-55408351 | Common:5; Rare:94 | ||||
| chr15:55408353-55408502 | Common:1; Rare:38 | ||||
| chr15:55498212-55498526 | Common:6; Rare:134; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:55993115-55993198 | Rare:21 | ||||
| chr15:55993234-55993495 | Common:3; Rare:86 | ||||
| chr15:55993511-55993747 | Common:2; Rare:82 | ||||
| chr15:56242980-56243185 | Common:1; Rare:57 | ||||
| chr15:56243376-56243552 | Rare:43 | ||||
| chr15:56243699-56243850 | Common:1; Rare:66 | ||||
| chr15:56244351-56244553 | Common:1; Rare:57 | ||||
| chr15:56365237-56365608 | Common:2; Rare:173 | ||||
| chr15:56464999-56465364 | Common:4; Rare:108 | ||||
| chr15:56733156-56733693 | Common:2; Rare:220 |