| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29073562-29073856 | Common:2; Rare:92 | ||||
| chr21:29298649-29298971 | Common:3; Rare:133 | ||||
| chr21:29300051-29300133 | Rare:15 | ||||
| chr21:29300271-29300421 | Rare:40 | ||||
| chr21:31659502-31659833 | Common:2; Rare:148; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr21:32279017-32279175 | Common:2; Rare:73 | ||||
| chr21:32298529-32298830 | Common:2; Rare:70 | ||||
| chr21:32298838-32299068 | Rare:86; Clinvar (pathogenic):1 | ||||
| chr21:32392906-32393179 | Common:2; Rare:114 | ||||
| chr21:32411591-32411835 | Rare:57 | ||||
| chr21:32412662-32412853 | Rare:49 | ||||
| chr21:32612224-32612480 | Common:3; Rare:70 | ||||
| chr21:32612544-32612899 | Rare:89 | ||||
| chr21:32727897-32728133 | Rare:117; Clinvar:2 | ||||
| chr21:32771707-32772167 | Common:13; Rare:203 |