| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39380188-39380480 | Common:1; Rare:134 | ||||
| chr21:39387632-39387815 | Common:2; Rare:77 | ||||
| chr21:39445729-39445949 | Common:3; Rare:68 | ||||
| chr21:41236427-41236626 | Rare:49 | ||||
| chr21:41252281-41252499 | Common:2; Rare:47 | ||||
| chr21:41766966-41767183 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr21:41879308-41879546 | Common:5; Rare:78 | ||||
| chr21:42878977-42879158 | Common:2; Rare:53 | ||||
| chr21:42879527-42879669 | Common:3; Rare:47 | ||||
| chr21:42893004-42893361 | Common:5; Rare:126 | ||||
| chr21:43659461-43659631 | Common:1; Rare:55 | ||||
| chr21:43776258-43776650 | Common:4; Rare:138; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr21:43789375-43789642 | Common:1; Rare:101 | ||||
| chr21:44299992-44300114 | Rare:51; Clinvar (benign):1 | ||||
| chr21:44339226-44339493 | Common:3; Rare:76 |