| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42120977-42121127 | Common:1; Rare:43 | ||||
| chr21:42878990-42879158 | Common:2; Rare:50 | ||||
| chr21:42879262-42879296 | Rare:14 | ||||
| chr21:42879527-42879674 | Common:3; Rare:48 | ||||
| chr21:42893042-42893342 | Common:4; Rare:100 | ||||
| chr21:43659461-43659644 | Common:1; Rare:59 | ||||
| chr21:43789369-43789602 | Common:1; Rare:78 | ||||
| chr21:44299984-44300112 | Rare:52; Clinvar (benign):1 | ||||
| chr21:44801774-44801890 | Rare:45 | ||||
| chr21:44873634-44874050 | Common:8; Rare:165 | ||||
| chr21:45287879-45288060 | Common:5; Rare:68 | ||||
| chr21:46184429-46184708 | Common:3; Rare:23 | ||||
| chr21:46286256-46286396 | Common:4; Rare:52 | ||||
| chr21:46323801-46324202 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46324459-46324653 | Common:3; Rare:73 |