| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:73632309-73632852 | Common:2; Rare:108 | ||||
| chr15:73633202-73633595 | Common:2; Rare:155 | ||||
| chr15:73684633-73684788 | Common:1; Rare:36 | ||||
| chr15:73699294-73699633 | Common:2; Rare:72 | ||||
| chr15:73925637-73925794 | Rare:21 | ||||
| chr15:73926206-73926792 | Common:1; Rare:125 | ||||
| chr15:73994619-73994871 | Rare:59 | ||||
| chr15:74433914-74434094 | Common:3; Rare:53 | ||||
| chr15:74461023-74461314 | Common:1; Rare:85 | ||||
| chr15:74540915-74541348 | Common:6; Rare:153 | ||||
| chr15:74541527-74541774 | Common:3; Rare:56 | ||||
| chr15:74615594-74615902 | Common:4; Rare:100 | ||||
| chr15:74628614-74629032 | Common:1; Rare:97 | ||||
| chr15:74782487-74782690 | Common:1; Rare:52 | ||||
| chr15:74889935-74890083 | Rare:61; Clinvar:1; Clinvar (pathogenic):1 |