| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30425797-30425856 | Common:1; Rare:13 | ||||
| chr22:30607092-30607328 | Common:1; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:31081283-31081345 | Rare:24 | ||||
| chr22:31107424-31107744 | Common:2; Rare:103 | ||||
| chr22:31160112-31160288 | Common:1; Rare:62 | ||||
| chr22:31212075-31212346 | Rare:92 | ||||
| chr22:31248130-31248391 | Common:1; Rare:55 | ||||
| chr22:31290689-31290911 | Rare:91 | ||||
| chr22:31292425-31292623 | Common:1; Rare:39 | ||||
| chr22:31399340-31399701 | Common:2; Rare:110 | ||||
| chr22:31489744-31490139 | Common:3; Rare:159 | ||||
| chr22:31496384-31496556 | Common:1; Rare:45 | ||||
| chr22:31630758-31631078 | Common:7; Rare:82 | ||||
| chr22:31638457-31638619 | Common:3; Rare:26 | ||||
| chr22:31662171-31662377 | Common:2; Rare:85 |