| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:17594982-17595176 | Common:2; Rare:35 | ||||
| chr21:17941313-17941437 | Common:1; Rare:15 | ||||
| chr21:25373523-25373878 | Common:5; Rare:32 | ||||
| chr21:25592756-25592826 | Common:2; Rare:19 | ||||
| chr21:26010675-26010749 | Common:1; Rare:13 | ||||
| chr21:26013052-26013222 | Common:1; Rare:30 | ||||
| chr21:26482949-26483104 | Common:2; Rare:30 | ||||
| chr21:29002694-29002797 | Common:2; Rare:36 | ||||
| chr21:29034561-29034864 | Common:1; Rare:57 | ||||
| chr21:31667072-31667274 | Rare:42; Clinvar (pathogenic):2 | ||||
| chr21:33232694-33232944 | Rare:39 | ||||
| chr21:33362304-33362558 | Rare:44 | ||||
| chr21:33527142-33527442 | Common:2; Rare:63 | ||||
| chr21:33945809-33945896 | Common:1; Rare:9 | ||||
| chr21:33968394-33968498 | Common:1; Rare:22 |