| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:64079924-64080109 | Common:2; Rare:77 | ||||
| chr21:14383167-14383486 | Common:2; Rare:76 | ||||
| chr21:17819324-17819488 | Common:1; Rare:58 | ||||
| chr21:17819640-17819698 | Rare:20 | ||||
| chr21:25607455-25607637 | Rare:85 | ||||
| chr21:25734851-25735435 | Common:3; Rare:207 | ||||
| chr21:26170617-26170926 | Common:5; Rare:101; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26845404-26845641 | Common:2; Rare:66 | ||||
| chr21:28992797-28993062 | Common:1; Rare:116 | ||||
| chr21:29019312-29019443 | Common:5; Rare:54 | ||||
| chr21:29024537-29024776 | Common:2; Rare:103 | ||||
| chr21:29024876-29025013 | Rare:26 | ||||
| chr21:29073576-29073888 | Common:2; Rare:101 | ||||
| chr21:31659522-31659745 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:32279017-32279281 | Common:3; Rare:99 |