| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31501990-31502300 | Rare:46 | ||||
| chr21:31525962-31526415 | Common:4; Rare:173 | ||||
| chr21:31529331-31530138 | Common:6; Rare:207 | ||||
| chr21:31531034-31531467 | Common:2; Rare:142 | ||||
| chr21:31557428-31558210 | Common:11; Rare:376 | ||||
| chr21:31666151-31666639 | Common:3; Rare:235; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr21:31668004-31668825 | Common:5; Rare:330; Clinvar (benign):3; Clinvar (pathogenic):14 | ||||
| chr21:31730457-31731300 | Common:4; Rare:415 | ||||
| chr21:31872360-31872690 | Rare:70 | ||||
| chr21:31908260-31908640 | Rare:81 | ||||
| chr21:32348540-32348876 | Common:5; Rare:67 | ||||
| chr21:32521512-32521729 | Common:1; Rare:42 | ||||
| chr21:32569428-32569744 | Common:2; Rare:62 | ||||
| chr21:33362196-33362472 | Common:1; Rare:56 | ||||
| chr21:33404243-33404498 | Common:1; Rare:49 |