| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74461101-74461329 | Rare:67 | ||||
| chr15:74540966-74541283 | Common:4; Rare:112 | ||||
| chr15:74615597-74615898 | Common:4; Rare:98 | ||||
| chr15:74842639-74842793 | Rare:36 | ||||
| chr15:74889812-74890080 | Rare:79; Clinvar (pathogenic):1 | ||||
| chr15:74957083-74957272 | Rare:56 | ||||
| chr15:75362370-75362707 | Rare:109 | ||||
| chr15:75368585-75368924 | Rare:90 | ||||
| chr15:75451740-75452065 | Common:1; Rare:73 | ||||
| chr15:75625612-75625822 | Common:2; Rare:49 | ||||
| chr15:75640164-75640531 | Common:2; Rare:115 | ||||
| chr15:75647683-75647950 | Common:2; Rare:59 | ||||
| chr15:75647974-75648212 | Common:1; Rare:52 | ||||
| chr15:75649529-75649646 | Rare:49 | ||||
| chr15:75649650-75649957 | Common:1; Rare:67 |