| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37916367-37916552 | Common:1; Rare:54 | ||||
| chr21:38498403-38498748 | Common:1; Rare:47 | ||||
| chr21:39183392-39183581 | Common:5; Rare:78 | ||||
| chr21:39445776-39445907 | Common:1; Rare:47 | ||||
| chr21:41426096-41426247 | Common:3; Rare:34 | ||||
| chr21:42496200-42496536 | Common:2; Rare:82 | ||||
| chr21:42514398-42514511 | Rare:23 | ||||
| chr21:42653463-42653806 | Common:5; Rare:53 | ||||
| chr21:42879554-42879665 | Common:2; Rare:28 | ||||
| chr21:42893050-42893336 | Common:4; Rare:92 | ||||
| chr21:42974201-42974649 | Common:1; Rare:161 | ||||
| chr21:43659461-43659623 | Common:1; Rare:52 | ||||
| chr21:43776257-43776584 | Common:4; Rare:114; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr21:43789378-43789624 | Common:1; Rare:91 | ||||
| chr21:44299992-44300106 | Rare:48; Clinvar (benign):1 |