| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26405819-26406055 | Common:1; Rare:66 | ||||
| chr21:26844723-26844804 | Common:1; Rare:37 | ||||
| chr21:29002697-29002826 | Common:1; Rare:44 | ||||
| chr21:29193035-29193468 | Common:8; Rare:111 | ||||
| chr21:30206908-30207143 | Rare:44 | ||||
| chr21:31666231-31666518 | Rare:66; Clinvar (pathogenic):1 | ||||
| chr21:32521548-32521717 | Common:1; Rare:31 | ||||
| chr21:33761781-33761970 | Common:2; Rare:46 | ||||
| chr21:36130328-36130455 | Common:1; Rare:36 | ||||
| chr21:36135564-36135779 | Common:2; Rare:47 | ||||
| chr21:36320783-36320865 | Rare:31 | ||||
| chr21:37221297-37221473 | Common:2; Rare:79 | ||||
| chr21:37563880-37563969 | Common:1; Rare:33 | ||||
| chr21:41186770-41187041 | Common:2; Rare:48 | ||||
| chr21:43600809-43601082 | Common:2; Rare:44 |