| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31496375-31496556 | Common:2; Rare:48 | ||||
| chr22:31662213-31662355 | Common:2; Rare:55 | ||||
| chr22:31750055-31750344 | Common:3; Rare:86 | ||||
| chr22:31753805-31753982 | Rare:58 | ||||
| chr22:31945358-31945413 | Common:1; Rare:12 | ||||
| chr22:35257406-35257501 | Common:1; Rare:25 | ||||
| chr22:35299716-35299931 | Common:2; Rare:58 | ||||
| chr22:35399905-35400164 | Rare:89 | ||||
| chr22:35840357-35840662 | Common:1; Rare:70 | ||||
| chr22:36387981-36388325 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr22:36529086-36529309 | Common:1; Rare:72 | ||||
| chr22:37199383-37199656 | Common:4; Rare:72 | ||||
| chr22:37608621-37608863 | Common:7; Rare:73 | ||||
| chr22:37849316-37849478 | Rare:91 | ||||
| chr22:37953532-37953797 | Common:1; Rare:99 |