| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26573108-26573327 | Rare:76 | ||||
| chr21:26845405-26845619 | Common:2; Rare:59 | ||||
| chr21:28885343-28885387 | Rare:33 | ||||
| chr21:28992797-28993130 | Common:2; Rare:138 | ||||
| chr21:29019307-29019443 | Common:5; Rare:58 | ||||
| chr21:29024530-29024726 | Common:2; Rare:86 | ||||
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073597-29073876 | Common:2; Rare:84 | ||||
| chr21:29298657-29298942 | Common:2; Rare:116 | ||||
| chr21:29939570-29939757 | Rare:44 | ||||
| chr21:29939760-29940128 | Common:5; Rare:86 | ||||
| chr21:31659502-31659787 | Common:2; Rare:131; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr21:32278970-32279219 | Common:3; Rare:113 | ||||
| chr21:32392912-32393179 | Common:2; Rare:113 | ||||
| chr21:32411595-32411772 | Rare:47 |