| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:17612827-17613037 | Common:1; Rare:90 | ||||
| chr21:17819311-17819532 | Common:1; Rare:81 | ||||
| chr21:25607419-25607545 | Common:1; Rare:72 | ||||
| chr21:25734855-25735504 | Common:5; Rare:222 | ||||
| chr21:25735644-25735768 | Common:1; Rare:29 | ||||
| chr21:26170565-26170890 | Common:3; Rare:107; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:28992788-28993103 | Common:2; Rare:131 | ||||
| chr21:29019289-29019434 | Common:5; Rare:57 | ||||
| chr21:29024537-29024753 | Common:2; Rare:98 | ||||
| chr21:29073541-29073856 | Common:2; Rare:101 | ||||
| chr21:29298734-29298948 | Common:2; Rare:94 | ||||
| chr21:31659514-31659838 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731951-31732140 | Common:2; Rare:79 | ||||
| chr21:32279010-32279155 | Common:1; Rare:65 | ||||
| chr21:32392894-32393179 | Common:2; Rare:118 |