| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656296-38656706 | Common:1; Rare:116 | ||||
| chr22:38681769-38682221 | Common:2; Rare:168 | ||||
| chr22:38754487-38754681 | Common:1; Rare:39 | ||||
| chr22:38794088-38794344 | Common:1; Rare:69 | ||||
| chr22:38872190-38872464 | Rare:73 | ||||
| chr22:39319578-39319896 | Common:4; Rare:122 | ||||
| chr22:39320280-39320353 | Common:1; Rare:12 | ||||
| chr22:39349798-39350004 | Common:1; Rare:65 | ||||
| chr22:39399646-39399811 | Common:3; Rare:67 | ||||
| chr22:39502138-39502417 | Rare:84 | ||||
| chr22:39532667-39533063 | Common:2; Rare:149 | ||||
| chr22:39533073-39533082 | Rare:3 | ||||
| chr22:40044121-40044362 | Common:2; Rare:56 | ||||
| chr22:40044527-40044870 | Common:2; Rare:81 | ||||
| chr22:40346398-40346578 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 |