| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42365599-42365868 | Common:3; Rare:53 | ||||
| chr21:42376280-42376598 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:42385723-42385941 | Common:2; Rare:44 | ||||
| chr21:42461205-42461410 | Common:2; Rare:37 | ||||
| chr21:42522149-42522335 | Common:3; Rare:41 | ||||
| chr21:42652952-42653125 | Common:2; Rare:34 | ||||
| chr21:42812607-42812821 | Common:1; Rare:36 | ||||
| chr21:42948849-42948923 | Common:2; Rare:18 | ||||
| chr21:43343164-43343434 | Common:3; Rare:46 | ||||
| chr21:43344417-43344732 | Common:2; Rare:86 | ||||
| chr21:43750357-43750514 | Common:1; Rare:46 | ||||
| chr21:44311151-44311254 | Common:1; Rare:37 | ||||
| chr21:44316265-44316524 | Common:3; Rare:92 | ||||
| chr21:44866787-44867052 | Common:2; Rare:43 | ||||
| chr21:45349859-45350263 | Common:4; Rare:82 |