| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37267910-37267979 | Rare:26 | ||||
| chr21:38805021-38805225 | Common:2; Rare:53 | ||||
| chr21:38805588-38805893 | Rare:73 | ||||
| chr21:38809838-38810111 | Common:2; Rare:48 | ||||
| chr21:39380188-39380483 | Common:1; Rare:135 | ||||
| chr21:39445751-39445913 | Common:3; Rare:53 | ||||
| chr21:41508059-41508349 | Common:2; Rare:62 | ||||
| chr21:41767014-41767176 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:42514418-42514556 | Rare:30 | ||||
| chr21:42879527-42879669 | Common:3; Rare:47 | ||||
| chr21:42893081-42893353 | Common:3; Rare:95 | ||||
| chr21:43659468-43659631 | Common:1; Rare:54 | ||||
| chr21:43776204-43776656 | Common:5; Rare:157; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789410-43789630 | Common:1; Rare:87 | ||||
| chr21:44299796-44300107 | Common:2; Rare:108; Clinvar (benign):1 |