| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74540952-74541262 | Common:3; Rare:106 | ||||
| chr15:74598335-74598524 | Common:1; Rare:83 | ||||
| chr15:74695983-74696056 | Rare:21 | ||||
| chr15:74873251-74873441 | Common:5; Rare:61 | ||||
| chr15:74889738-74890076 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr15:75347566-75347888 | Common:2; Rare:84 | ||||
| chr15:75451677-75452031 | Common:1; Rare:93 | ||||
| chr15:75455802-75455967 | Rare:51 | ||||
| chr15:75625579-75625829 | Common:2; Rare:62 | ||||
| chr15:76311366-76311652 | Common:1; Rare:99; Clinvar:6; Clinvar (benign):7 | ||||
| chr15:76905313-76905485 | Common:1; Rare:61 | ||||
| chr15:77420051-77420433 | Common:2; Rare:107 | ||||
| chr15:78149176-78149410 | Common:1; Rare:76 | ||||
| chr15:78299571-78299681 | Rare:47 | ||||
| chr15:78299710-78299745 | Rare:10 |