| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42514375-42514564 | Rare:38 | ||||
| chr21:42878962-42879151 | Common:2; Rare:54 | ||||
| chr21:42879520-42879680 | Common:3; Rare:53 | ||||
| chr21:42893064-42893361 | Common:4; Rare:105 | ||||
| chr21:42974218-42974621 | Common:1; Rare:154 | ||||
| chr21:43659461-43659592 | Common:1; Rare:44 | ||||
| chr21:43740800-43741035 | Common:5; Rare:78 | ||||
| chr21:43776204-43776377 | Common:2; Rare:65; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43776408-43776475 | Common:1; Rare:21 | ||||
| chr21:43789369-43789624 | Common:1; Rare:93 | ||||
| chr21:43925249-43925416 | Common:1; Rare:24 | ||||
| chr21:44299992-44300123 | Rare:52; Clinvar (benign):1 | ||||
| chr21:44339203-44339469 | Common:2; Rare:83 | ||||
| chr21:44353519-44353649 | Common:2; Rare:22 | ||||
| chr21:44801717-44801890 | Rare:68 |