| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41285973-41286075 | Common:1; Rare:31 | ||||
| chr22:41286122-41286437 | Common:2; Rare:103 | ||||
| chr22:41301159-41301637 | Common:2; Rare:128 | ||||
| chr22:41468657-41468751 | Common:2; Rare:30 | ||||
| chr22:41468990-41469144 | Rare:47 | ||||
| chr22:41544330-41544729 | Common:10; Rare:136 | ||||
| chr22:41560874-41561136 | Common:9; Rare:70 | ||||
| chr22:41621009-41621370 | Common:7; Rare:133 | ||||
| chr22:41947091-41947243 | Rare:55 | ||||
| chr22:42070761-42071047 | Common:3; Rare:65 | ||||
| chr22:42090735-42090984 | Common:1; Rare:88; Clinvar (pathogenic):1 | ||||
| chr22:42614850-42615244 | Common:3; Rare:161 | ||||
| chr22:42649303-42649459 | Common:1; Rare:65 | ||||
| chr22:43955326-43955581 | Common:3; Rare:79 | ||||
| chr22:45163682-45163952 | Common:4; Rare:91 |