| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:22509152-22509278 | Rare:20 | ||||
| chr22:22520274-22520475 | Common:6; Rare:41 | ||||
| chr22:22558987-22559354 | Common:1; Rare:113 | ||||
| chr22:22644515-22644679 | Common:5; Rare:7 | ||||
| chr22:23141942-23142177 | Common:5; Rare:65 | ||||
| chr22:23145171-23145546 | Common:3; Rare:121 | ||||
| chr22:23580149-23580594 | Common:4; Rare:114; Clinvar:1 | ||||
| chr22:23631971-23632277 | Common:3; Rare:62 | ||||
| chr22:23632298-23632342 | Rare:6 | ||||
| chr22:23632346-23632443 | Common:1; Rare:16 | ||||
| chr22:23688042-23688141 | Rare:22 | ||||
| chr22:23767940-23767995 | Rare:16 | ||||
| chr22:23786802-23787186 | Common:4; Rare:132; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:23838983-23839065 | Rare:35 | ||||
| chr22:23857793-23857920 | Common:2; Rare:41 |