| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:22508694-22508913 | Rare:73 | ||||
| chr22:22520266-22520455 | Common:4; Rare:40 | ||||
| chr22:22559213-22559342 | Rare:45 | ||||
| chr22:23767930-23768054 | Rare:32 | ||||
| chr22:23786873-23787061 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:23857619-23857920 | Common:2; Rare:106 | ||||
| chr22:23894308-23894582 | Common:3; Rare:107 | ||||
| chr22:24011110-24011454 | Common:40; Rare:190 | ||||
| chr22:24270632-24270971 | Common:3; Rare:120 | ||||
| chr22:24271065-24271181 | Common:2; Rare:53 | ||||
| chr22:24555070-24555507 | Common:4; Rare:162 | ||||
| chr22:24555817-24556080 | Rare:81 | ||||
| chr22:24607522-24607718 | Common:2; Rare:49 | ||||
| chr22:24952593-24952748 | Rare:45 | ||||
| chr22:26483757-26483967 | Common:4; Rare:89; Clinvar:5; Clinvar (benign):1 |