| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019312-29019414 | Common:5; Rare:42 | ||||
| chr21:29024526-29024747 | Common:2; Rare:98 | ||||
| chr21:29024876-29025039 | Rare:31 | ||||
| chr21:29073586-29073870 | Common:2; Rare:85 | ||||
| chr21:29298584-29298935 | Common:2; Rare:132 | ||||
| chr21:29939662-29939957 | Common:3; Rare:61 | ||||
| chr21:29939982-29940091 | Rare:30 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732062-31732407 | Common:5; Rare:148 | ||||
| chr21:32279010-32279214 | Common:3; Rare:86 | ||||
| chr21:32392965-32393163 | Common:2; Rare:85 | ||||
| chr21:32612549-32612903 | Rare:88 | ||||
| chr21:32727844-32728167 | Rare:145; Clinvar:2 | ||||
| chr21:32771730-32772167 | Common:13; Rare:192 | ||||
| chr21:33266262-33266473 | Rare:68; Clinvar:3 |