| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019312-29019407 | Common:5; Rare:38 | ||||
| chr21:29024526-29024730 | Common:2; Rare:89 | ||||
| chr21:29073586-29073854 | Common:2; Rare:80 | ||||
| chr21:29298734-29298950 | Common:2; Rare:95 | ||||
| chr21:31659502-31659835 | Common:2; Rare:149; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732061-31732449 | Common:5; Rare:162 | ||||
| chr21:32279016-32279214 | Common:3; Rare:85 | ||||
| chr21:32392917-32393163 | Common:2; Rare:104 | ||||
| chr21:32411589-32411791 | Rare:51 | ||||
| chr21:32612514-32612884 | Rare:90 | ||||
| chr21:32727897-32728122 | Rare:110; Clinvar:2 | ||||
| chr21:32771707-32772171 | Common:13; Rare:204 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324750-33325073 | Common:4; Rare:122 | ||||
| chr21:33479854-33480190 | Common:1; Rare:112 |