| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133243561-133243714 | Rare:23 | ||||
| chr8:133246594-133246686 | Rare:23; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:133254108-133254306 | Common:2; Rare:37 | ||||
| chr8:133273891-133274085 | Common:4; Rare:42 | ||||
| chr8:133280221-133280391 | Common:1; Rare:58; Clinvar (benign):4 | ||||
| chr8:133323200-133323277 | Common:1; Rare:13 | ||||
| chr8:133358955-133359228 | Common:3; Rare:53 | ||||
| chr8:135536267-135536332 | Rare:10 | ||||
| chr8:140697171-140697322 | Common:1; Rare:23 | ||||
| chr8:140724700-140724828 | Common:2; Rare:22 | ||||
| chr8:140725974-140726016 | Rare:7 | ||||
| chr8:140727389-140727623 | Common:1; Rare:41 | ||||
| chr8:140826609-140826751 | Rare:33 | ||||
| chr8:140963542-140963586 | Rare:10 | ||||
| chr8:140964019-140964074 | Common:1; Rare:9 |