| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30591828-30592217 | Common:5; Rare:114 | ||||
| chr22:30607038-30607373 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):3 | ||||
| chr22:31081175-31081456 | Common:2; Rare:75 | ||||
| chr22:31084866-31084991 | Rare:34 | ||||
| chr22:31107417-31107982 | Common:2; Rare:160 | ||||
| chr22:31122292-31122651 | Common:1; Rare:44 | ||||
| chr22:31122658-31122776 | Common:1; Rare:23 | ||||
| chr22:31122787-31123105 | Common:2; Rare:92 | ||||
| chr22:31160092-31160282 | Common:1; Rare:67 | ||||
| chr22:31290668-31290915 | Rare:106 | ||||
| chr22:31292374-31292618 | Common:1; Rare:53 | ||||
| chr22:31399452-31399702 | Rare:74 | ||||
| chr22:31489768-31490164 | Common:3; Rare:159 | ||||
| chr22:31496400-31496565 | Common:1; Rare:40 | ||||
| chr22:31630768-31630976 | Common:5; Rare:58 |