| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29073586-29073865 | Common:2; Rare:82 | ||||
| chr21:29076828-29077114 | Common:2; Rare:66 | ||||
| chr21:29298551-29298947 | Common:3; Rare:147 | ||||
| chr21:29300059-29300159 | Rare:22 | ||||
| chr21:31659502-31659833 | Common:2; Rare:148; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr21:32279010-32279219 | Common:3; Rare:87 | ||||
| chr21:32392906-32393171 | Common:2; Rare:111 | ||||
| chr21:32411595-32411815 | Rare:55 | ||||
| chr21:32612319-32612659 | Rare:85 | ||||
| chr21:32727885-32728170 | Rare:136; Clinvar:2 | ||||
| chr21:32771707-32772241 | Common:14; Rare:227 | ||||
| chr21:33229739-33230157 | Common:8; Rare:162 | ||||
| chr21:33265758-33265949 | Rare:37 | ||||
| chr21:33266255-33266473 | Rare:68; Clinvar:3 | ||||
| chr21:33324854-33325073 | Common:4; Rare:92 |