| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42878967-42879166 | Common:2; Rare:60 | ||||
| chr21:42879499-42879676 | Common:3; Rare:67 | ||||
| chr21:42893004-42893370 | Common:5; Rare:130 | ||||
| chr21:42974367-42974646 | Common:1; Rare:103 | ||||
| chr21:43659443-43659644 | Common:1; Rare:66 | ||||
| chr21:43776207-43776585 | Common:5; Rare:129; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789094-43789128 | Rare:5 | ||||
| chr21:43789375-43789632 | Common:1; Rare:95 | ||||
| chr21:44299992-44300112 | Rare:50; Clinvar (benign):1 | ||||
| chr21:44339225-44339508 | Common:3; Rare:79 | ||||
| chr21:44425590-44425735 | Rare:61 | ||||
| chr21:44801739-44801897 | Rare:69 | ||||
| chr21:44817964-44818170 | Common:1; Rare:79 | ||||
| chr21:44873618-44874050 | Common:8; Rare:174 | ||||
| chr21:44939871-44940092 | Common:2; Rare:63 |