| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024508-29024730 | Common:3; Rare:91 | ||||
| chr21:29073562-29073850 | Common:2; Rare:89 | ||||
| chr21:29298657-29298935 | Common:2; Rare:112 | ||||
| chr21:31659531-31659838 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732061-31732343 | Common:5; Rare:131 | ||||
| chr21:32279010-32279315 | Common:3; Rare:105 | ||||
| chr21:32392945-32393191 | Common:4; Rare:106 | ||||
| chr21:32411634-32411815 | Rare:43 | ||||
| chr21:32412347-32412737 | Common:2; Rare:85 | ||||
| chr21:32612514-32612883 | Rare:89 | ||||
| chr21:32727897-32728129 | Rare:115; Clinvar:2 | ||||
| chr21:32771707-32771825 | Rare:60 | ||||
| chr21:32771836-32772167 | Common:13; Rare:138 | ||||
| chr21:33266262-33266462 | Rare:65; Clinvar:3 | ||||
| chr21:33324847-33325088 | Common:4; Rare:105 |