| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39349460-39349717 | Common:2; Rare:85 | ||||
| chr21:39380405-39380423 | Rare:3 | ||||
| chr21:39387680-39387806 | Common:2; Rare:54 | ||||
| chr21:39445740-39445878 | Common:3; Rare:43 | ||||
| chr21:42879467-42879665 | Common:3; Rare:83 | ||||
| chr21:42893004-42893378 | Common:5; Rare:133 | ||||
| chr21:43659461-43659592 | Common:1; Rare:44 | ||||
| chr21:43745335-43745482 | Common:2; Rare:27 | ||||
| chr21:43776281-43776657 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):6 | ||||
| chr21:44299979-44300114 | Rare:55; Clinvar (benign):1 | ||||
| chr21:44339224-44339552 | Common:3; Rare:90 | ||||
| chr21:44425567-44425714 | Common:1; Rare:60 | ||||
| chr21:44801713-44801893 | Rare:70 | ||||
| chr21:44865272-44865416 | Common:1; Rare:46 | ||||
| chr21:44873504-44873554 | Rare:14 |