| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31662204-31662337 | Common:1; Rare:53 | ||||
| chr22:31753820-31754107 | Common:1; Rare:102 | ||||
| chr22:35299726-35299931 | Common:2; Rare:53 | ||||
| chr22:35300108-35300320 | Rare:61 | ||||
| chr22:35399910-35400197 | Rare:100 | ||||
| chr22:36239982-36240189 | Rare:38 | ||||
| chr22:36252991-36253152 | Rare:33 | ||||
| chr22:36387931-36388327 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481565-36481729 | Common:2; Rare:45 | ||||
| chr22:36529105-36529529 | Common:6; Rare:130 | ||||
| chr22:37019427-37019721 | Common:1; Rare:87 | ||||
| chr22:37199383-37199612 | Common:4; Rare:54 | ||||
| chr22:37560331-37560538 | Common:1; Rare:70 | ||||
| chr22:37608679-37609052 | Common:2; Rare:108 | ||||
| chr22:37676055-37676188 | Rare:20 |