| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42062687-42062895 | Common:1; Rare:59 | ||||
| chr21:42315407-42315684 | Common:1; Rare:85 | ||||
| chr21:42403724-42403935 | Common:1; Rare:44 | ||||
| chr21:42514428-42514498 | Rare:14 | ||||
| chr21:42653439-42653799 | Common:5; Rare:55 | ||||
| chr21:42879525-42879669 | Common:3; Rare:48 | ||||
| chr21:42893050-42893344 | Common:4; Rare:99 | ||||
| chr21:43659461-43659636 | Common:1; Rare:56 | ||||
| chr21:43789365-43789602 | Common:1; Rare:79 | ||||
| chr21:44089520-44089753 | Common:1; Rare:57 | ||||
| chr21:44299992-44300123 | Rare:52; Clinvar (benign):1 | ||||
| chr21:44339226-44339469 | Common:2; Rare:74 | ||||
| chr21:44353446-44353661 | Common:2; Rare:39 | ||||
| chr21:44801740-44801880 | Rare:63 | ||||
| chr21:44817963-44818287 | Common:1; Rare:134 |