| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42974993-42975279 | Common:10; Rare:204 | ||||
| chr21:43659376-43659662 | Common:3; Rare:229 | ||||
| chr21:43659813-43660213 | Common:2; Rare:134 | ||||
| chr21:43718749-43719503 | Common:24; Rare:511 | ||||
| chr21:43776187-43776810 | Common:15; Rare:446; Clinvar:12; Clinvar (benign):32; Clinvar (pathogenic):6 | ||||
| chr21:43788613-43789209 | Common:9; Rare:175 | ||||
| chr21:43789328-43789650 | Common:3; Rare:358 | ||||
| chr21:43865017-43865328 | Common:2; Rare:194 | ||||
| chr21:43950843-43950967 | Rare:19 | ||||
| chr21:44012095-44012476 | Common:6; Rare:328 | ||||
| chr21:44299532-44299781 | Common:2; Rare:113 | ||||
| chr21:44299862-44300191 | Common:3; Rare:251; Clinvar (benign):3 | ||||
| chr21:44300280-44300873 | Common:6; Rare:259 | ||||
| chr21:44339102-44339266 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:44339180-44339585 | Common:8; Rare:265 |