| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656348-38656741 | Common:1; Rare:104 | ||||
| chr22:38681771-38682439 | Common:3; Rare:226 | ||||
| chr22:38700926-38700997 | Rare:27 | ||||
| chr22:38754955-38755106 | Common:4; Rare:31 | ||||
| chr22:38982276-38982443 | Common:1; Rare:37 | ||||
| chr22:39318611-39318743 | Common:3; Rare:39 | ||||
| chr22:39319520-39319735 | Common:3; Rare:112 | ||||
| chr22:39319738-39319832 | Rare:27 | ||||
| chr22:39320370-39320471 | Common:2; Rare:26 | ||||
| chr22:39502158-39502418 | Rare:79 | ||||
| chr22:39520819-39521552 | Common:9; Rare:270 | ||||
| chr22:39532661-39532872 | Common:2; Rare:95 | ||||
| chr22:40346434-40346706 | Common:1; Rare:119; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40636629-40637003 | Common:2; Rare:109 | ||||
| chr22:40819267-40819529 | Common:11; Rare:120 |