| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41832656-41833560 | Common:8; Rare:432 | ||||
| chr22:41945960-41946370 | Common:2; Rare:154 | ||||
| chr22:41946695-41946979 | Common:6; Rare:148 | ||||
| chr22:41947078-41947267 | Common:2; Rare:125 | ||||
| chr22:41976600-41976950 | Rare:89 | ||||
| chr22:41998568-41998816 | Common:4; Rare:155 | ||||
| chr22:42070515-42070968 | Common:6; Rare:174; Clinvar:1 | ||||
| chr22:42074050-42074670 | Common:13; Rare:158 | ||||
| chr22:42079510-42079783 | Common:4; Rare:135 | ||||
| chr22:42090642-42091102 | Common:3; Rare:276; Clinvar (pathogenic):2 | ||||
| chr22:42343440-42344200 | Common:9; Rare:226 | ||||
| chr22:42519739-42519965 | Common:2; Rare:176 | ||||
| chr22:42614848-42615257 | Common:6; Rare:337 | ||||
| chr22:42649310-42649488 | Common:2; Rare:141 | ||||
| chr22:42720810-42721046 | Common:7; Rare:131 |