| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41620958-41621420 | Common:7; Rare:162 | ||||
| chr22:41621581-41621809 | Common:2; Rare:67 | ||||
| chr22:41800528-41800646 | Rare:37 | ||||
| chr22:41832909-41833221 | Common:3; Rare:104 | ||||
| chr22:42070646-42070977 | Common:4; Rare:76 | ||||
| chr22:42079491-42079807 | Common:2; Rare:89 | ||||
| chr22:42090607-42091001 | Common:2; Rare:167; Clinvar (pathogenic):1 | ||||
| chr22:42553802-42553923 | Rare:36 | ||||
| chr22:42614826-42615259 | Common:3; Rare:194 | ||||
| chr22:42644593-42644823 | Common:7; Rare:55 | ||||
| chr22:42649329-42649482 | Common:1; Rare:60 | ||||
| chr22:42857177-42857467 | Common:3; Rare:122 | ||||
| chr22:42959818-42959987 | Common:1; Rare:30 | ||||
| chr22:42960214-42960413 | Common:2; Rare:30 | ||||
| chr22:43015044-43015384 | Common:2; Rare:132 |