| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42491013-42491220 | Common:1; Rare:65 | ||||
| chr15:42495517-42495694 | Common:2; Rare:54 | ||||
| chr15:42548733-42548875 | Common:1; Rare:83 | ||||
| chr15:43106018-43106175 | Rare:47 | ||||
| chr15:43330536-43330694 | Rare:59 | ||||
| chr15:43371030-43371231 | Common:1; Rare:42 | ||||
| chr15:43493080-43493287 | Rare:61 | ||||
| chr15:43510670-43511137 | Rare:181 | ||||
| chr15:43517492-43517659 | Common:2; Rare:42 | ||||
| chr15:43777116-43777403 | Rare:65 | ||||
| chr15:44427269-44427653 | Common:1; Rare:96 | ||||
| chr15:44536855-44537196 | Common:1; Rare:120 | ||||
| chr15:44711341-44711610 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728846-44729146 | Common:1; Rare:61 | ||||
| chr15:45023052-45023233 | Common:3; Rare:47 |