| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42010293-42010487 | Common:2; Rare:57 | ||||
| chr21:42496207-42496536 | Common:2; Rare:78 | ||||
| chr21:42514428-42514545 | Rare:26 | ||||
| chr21:42879527-42879674 | Common:3; Rare:48 | ||||
| chr21:42893059-42893365 | Common:4; Rare:108 | ||||
| chr21:43659468-43659592 | Common:1; Rare:43 | ||||
| chr21:43776200-43776379 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43925335-43925440 | Common:1; Rare:9 | ||||
| chr21:44299981-44300108 | Rare:51; Clinvar (benign):1 | ||||
| chr21:44540213-44540412 | Common:2; Rare:47 | ||||
| chr21:44551511-44551694 | Common:3; Rare:46 | ||||
| chr21:44600346-44600564 | Common:7; Rare:43 | ||||
| chr21:44801707-44801872 | Rare:66 | ||||
| chr21:44873626-44874050 | Common:8; Rare:170 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 |