| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74725860-74726170 | Common:3; Rare:74 | ||||
| chr15:74781895-74782135 | Common:3; Rare:78 | ||||
| chr15:74842500-74842830 | Rare:80 | ||||
| chr15:74843124-74843360 | Common:1; Rare:62 | ||||
| chr15:74872923-74873159 | Common:1; Rare:66 | ||||
| chr15:74873321-74873523 | Common:6; Rare:54 | ||||
| chr15:74889907-74890125 | Rare:84; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74905723-74906051 | Rare:47 | ||||
| chr15:74906769-74906943 | Common:1; Rare:74 | ||||
| chr15:74938031-74938280 | Common:2; Rare:87 | ||||
| chr15:74956763-74956887 | Common:1; Rare:50 | ||||
| chr15:74995324-74995603 | Common:5; Rare:99 | ||||
| chr15:75023410-75023697 | Common:3; Rare:70 | ||||
| chr15:75201740-75201917 | Rare:58 | ||||
| chr15:75335938-75336114 | Common:2; Rare:88 |