| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41947111-41947231 | Rare:39 | ||||
| chr22:42079491-42079757 | Common:2; Rare:69 | ||||
| chr22:42090736-42090947 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
| chr22:42553676-42553967 | Common:1; Rare:88 | ||||
| chr22:42614850-42615246 | Common:3; Rare:164 | ||||
| chr22:42649316-42649453 | Common:1; Rare:60 | ||||
| chr22:43143366-43143479 | Common:2; Rare:32 | ||||
| chr22:43151442-43151588 | Common:2; Rare:34 | ||||
| chr22:43955268-43955528 | Common:3; Rare:74 | ||||
| chr22:44024130-44024335 | Common:2; Rare:68 | ||||
| chr22:44025764-44026019 | Common:1; Rare:57 | ||||
| chr22:44180836-44181033 | Common:1; Rare:37 | ||||
| chr22:44181236-44181436 | Common:3; Rare:51 | ||||
| chr22:46053735-46053864 | Rare:53 | ||||
| chr22:46250262-46250396 | Common:2; Rare:39 |