| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26845291-26845649 | Common:2; Rare:103 | ||||
| chr21:28885337-28885431 | Common:2; Rare:71 | ||||
| chr21:28992773-28993152 | Common:2; Rare:155 | ||||
| chr21:29019312-29019443 | Common:5; Rare:54 | ||||
| chr21:29024534-29024738 | Common:2; Rare:92 | ||||
| chr21:29073586-29073909 | Common:2; Rare:103 | ||||
| chr21:31659483-31659806 | Common:2; Rare:145; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr21:32279016-32279214 | Common:3; Rare:85 | ||||
| chr21:32392984-32393171 | Common:2; Rare:77 | ||||
| chr21:32612260-32612932 | Common:1; Rare:175 | ||||
| chr21:32771715-32772163 | Common:13; Rare:199 | ||||
| chr21:33266262-33266473 | Rare:68; Clinvar:3 | ||||
| chr21:33324862-33325065 | Common:4; Rare:85 | ||||
| chr21:33403290-33403579 | Common:1; Rare:70 | ||||
| chr21:33479805-33480121 | Rare:107 |