| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21629963-21630275 | Common:2; Rare:103 | ||||
| chr22:21642033-21642402 | Common:4; Rare:221 | ||||
| chr22:21665901-21666070 | Rare:93 | ||||
| chr22:21666084-21666484 | Common:4; Rare:197 | ||||
| chr22:21867554-21867823 | Common:5; Rare:133 | ||||
| chr22:21952809-21952961 | Common:1; Rare:57 | ||||
| chr22:21982729-21982871 | Rare:40 | ||||
| chr22:22508700-22509050 | Common:1; Rare:172 | ||||
| chr22:22558992-22559363 | Common:1; Rare:118 | ||||
| chr22:23069860-23070530 | Common:7; Rare:385 | ||||
| chr22:23180340-23180568 | Common:2; Rare:87 | ||||
| chr22:23180724-23180853 | Common:5; Rare:55 | ||||
| chr22:23750976-23751218 | Common:3; Rare:128 | ||||
| chr22:23767819-23768350 | Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:23786869-23787061 | Common:3; Rare:139; Clinvar:6; Clinvar (benign):2 |