| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26845210-26845716 | Common:6; Rare:260 | ||||
| chr21:28885233-28885450 | Common:9; Rare:275 | ||||
| chr21:28992748-28993218 | Common:6; Rare:447 | ||||
| chr21:29019226-29019497 | Common:15; Rare:248 | ||||
| chr21:29024332-29024747 | Common:8; Rare:329 | ||||
| chr21:29024781-29025140 | Common:4; Rare:198 | ||||
| chr21:29073565-29073936 | Common:6; Rare:317 | ||||
| chr21:29194401-29194635 | Common:2; Rare:33 | ||||
| chr21:29298670-29298985 | Common:5; Rare:342 | ||||
| chr21:29299010-29299220 | Rare:117 | ||||
| chr21:31344133-31344375 | Common:1; Rare:55 | ||||
| chr21:31558987-31559320 | Common:8; Rare:271 | ||||
| chr21:31559360-31559731 | Common:2; Rare:274 | ||||
| chr21:31559913-31560144 | Common:3; Rare:129 | ||||
| chr21:31659459-31659842 | Common:6; Rare:455; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):16 |