| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:28048321-28048451 | Common:2; Rare:22 | ||||
| chr21:28090080-28090410 | Common:5; Rare:79 | ||||
| chr21:29002753-29002816 | Common:1; Rare:28 | ||||
| chr21:31666304-31666507 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr21:31668388-31668513 | Rare:39; Clinvar (pathogenic):1 | ||||
| chr21:33976217-33976511 | Common:7; Rare:63 | ||||
| chr21:36430102-36430334 | Common:2; Rare:46 | ||||
| chr21:39452628-39452788 | Common:1; Rare:24 | ||||
| chr21:45349852-45350132 | Common:1; Rare:49 | ||||
| chr21:46356605-46356916 | Common:3; Rare:64 | ||||
| chr21:46374834-46375215 | Common:2; Rare:98 | ||||
| chr22:17037173-17037275 | Common:1; Rare:24 | ||||
| chr22:21044997-21045206 | Common:1; Rare:39 | ||||
| chr22:22298058-22298210 | Common:2; Rare:56 | ||||
| chr22:25111341-25111451 | Rare:26 |