| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41475947-41476316 | Common:5; Rare:65 | ||||
| chr22:41666775-41667013 | Common:1; Rare:76 | ||||
| chr22:41747180-41747415 | Common:1; Rare:45 | ||||
| chr22:41862292-41862492 | Rare:35 | ||||
| chr22:41862786-41863061 | Common:1; Rare:57 | ||||
| chr22:41919193-41919434 | Common:2; Rare:38 | ||||
| chr22:41919832-41920167 | Common:2; Rare:83 | ||||
| chr22:41921926-41921945 | |||||
| chr22:41924368-41924589 | Common:3; Rare:41 | ||||
| chr22:41924893-41925122 | Rare:37 | ||||
| chr22:41925520-41925918 | Common:4; Rare:98 | ||||
| chr22:41925921-41926137 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41936429-41936619 | Common:1; Rare:37 | ||||
| chr22:41945793-41945871 | Rare:10 | ||||
| chr22:41945885-41946065 | Common:1; Rare:52 |