| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39445757-39445919 | Common:3; Rare:52 | ||||
| chr21:41361965-41362039 | Rare:11 | ||||
| chr21:41426075-41426325 | Common:3; Rare:52 | ||||
| chr21:42653473-42653817 | Common:5; Rare:55 | ||||
| chr21:42731619-42731904 | Rare:82 | ||||
| chr21:42879532-42879669 | Common:3; Rare:43 | ||||
| chr21:42893081-42893354 | Common:3; Rare:96 | ||||
| chr21:43659461-43659631 | Common:1; Rare:55 | ||||
| chr21:44299992-44300123 | Rare:52; Clinvar (benign):1 | ||||
| chr21:44339226-44339466 | Common:2; Rare:72 | ||||
| chr21:44801729-44801904 | Rare:74 | ||||
| chr21:44873479-44874063 | Common:9; Rare:221 | ||||
| chr21:44939913-44940060 | Common:2; Rare:43 | ||||
| chr21:45074461-45074771 | Common:3; Rare:149 | ||||
| chr21:45287858-45288106 | Common:6; Rare:99 |