| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23772501-23772946 | Common:2; Rare:211 | ||||
| chr22:23786696-23787209 | Common:9; Rare:313; Clinvar:14; Clinvar (benign):9 | ||||
| chr22:23787197-23787550 | Common:21; Rare:307; Clinvar:2; Clinvar (benign):10 | ||||
| chr22:23856677-23856979 | Common:3; Rare:71 | ||||
| chr22:23857617-23857978 | Common:10; Rare:340 | ||||
| chr22:23893740-23894002 | Rare:96 | ||||
| chr22:23894003-23894746 | Common:14; Rare:454 | ||||
| chr22:24010933-24011505 | Common:127; Rare:674 | ||||
| chr22:24155551-24156057 | Common:2; Rare:182 | ||||
| chr22:24156946-24157290 | Rare:116 | ||||
| chr22:24181359-24181582 | Common:2; Rare:70 | ||||
| chr22:24270528-24271213 | Common:14; Rare:502 | ||||
| chr22:24303390-24303940 | Common:5; Rare:99 | ||||
| chr22:24555014-24555495 | Common:8; Rare:319 | ||||
| chr22:24555614-24556081 | Rare:215 |