| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26840523-26840691 | Common:1; Rare:49 | ||||
| chr21:26842796-26843189 | Common:7; Rare:72 | ||||
| chr21:26844189-26844412 | Common:3; Rare:79 | ||||
| chr21:26845169-26845609 | Common:2; Rare:119 | ||||
| chr21:28885337-28885425 | Common:2; Rare:68 | ||||
| chr21:28992773-28993060 | Common:1; Rare:124 | ||||
| chr21:29024526-29024738 | Common:2; Rare:93 | ||||
| chr21:29024876-29024991 | Rare:20 | ||||
| chr21:29073541-29073850 | Common:2; Rare:98 | ||||
| chr21:29298520-29298942 | Common:2; Rare:153 | ||||
| chr21:31659522-31659833 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr21:32279010-32279214 | Common:3; Rare:86 | ||||
| chr21:32392873-32393197 | Common:4; Rare:133 | ||||
| chr21:32411593-32411815 | Rare:55 | ||||
| chr21:32412234-32412519 | Common:2; Rare:66 |