| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42878907-42879210 | Common:2; Rare:91 | ||||
| chr21:42879478-42879745 | Common:3; Rare:97 | ||||
| chr21:42892935-42893474 | Common:7; Rare:180 | ||||
| chr21:42893519-42893681 | Rare:45 | ||||
| chr21:42893718-42893830 | Rare:28 | ||||
| chr21:42974086-42974767 | Common:1; Rare:226 | ||||
| chr21:42974964-42975177 | Common:4; Rare:70 | ||||
| chr21:43659433-43659666 | Common:1; Rare:77 | ||||
| chr21:43659823-43659889 | Rare:28 | ||||
| chr21:43659970-43660018 | Rare:8 | ||||
| chr21:43718901-43719231 | Common:7; Rare:107 | ||||
| chr21:43719397-43719509 | Common:1; Rare:27 | ||||
| chr21:43719537-43719775 | Common:2; Rare:57 | ||||
| chr21:43728735-43728906 | Common:1; Rare:49 | ||||
| chr21:43776257-43776690 | Common:4; Rare:148; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 |