| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41416890-41417202 | Common:4; Rare:129 | ||||
| chr15:41660321-41660521 | Rare:69 | ||||
| chr15:41972447-41972793 | Common:2; Rare:101 | ||||
| chr15:42208263-42208404 | Rare:49 | ||||
| chr15:42273395-42273487 | Rare:36 | ||||
| chr15:42491036-42491214 | Common:1; Rare:57 | ||||
| chr15:42495508-42495725 | Common:2; Rare:65 | ||||
| chr15:42548700-42548892 | Common:2; Rare:102 | ||||
| chr15:43106023-43106226 | Rare:65 | ||||
| chr15:43330594-43330711 | Rare:41 | ||||
| chr15:43371043-43371108 | Rare:13 | ||||
| chr15:43648737-43649027 | Common:3; Rare:125 | ||||
| chr15:43746285-43746587 | Common:1; Rare:129 | ||||
| chr15:44536657-44537206 | Common:1; Rare:168 | ||||
| chr15:44711252-44711611 | Rare:99; Clinvar:1; Clinvar (pathogenic):1 |