| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024539-29024726 | Common:2; Rare:82 | ||||
| chr21:29073586-29073852 | Common:2; Rare:79 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279010-32279206 | Common:3; Rare:85 | ||||
| chr21:32298635-32298965 | Common:2; Rare:91 | ||||
| chr21:32392940-32393171 | Common:2; Rare:98 | ||||
| chr21:32411600-32411786 | Rare:46 | ||||
| chr21:32412395-32412741 | Common:2; Rare:74 | ||||
| chr21:32612544-32612890 | Rare:87 | ||||
| chr21:32727897-32728133 | Rare:117; Clinvar:2 | ||||
| chr21:32771707-32772167 | Common:13; Rare:203 | ||||
| chr21:33266262-33266462 | Rare:65; Clinvar:3 | ||||
| chr21:33324833-33325058 | Common:4; Rare:96 | ||||
| chr21:33403331-33403544 | Common:1; Rare:56 | ||||
| chr21:33479854-33480167 | Common:1; Rare:105 |