| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41767050-41767167 | Common:3; Rare:55; Clinvar:1 | ||||
| chr21:42653473-42653789 | Common:5; Rare:49 | ||||
| chr21:42893050-42893342 | Common:4; Rare:97 | ||||
| chr21:43659461-43659585 | Common:1; Rare:41 | ||||
| chr21:43789369-43789611 | Common:1; Rare:85 | ||||
| chr21:44299992-44300096 | Rare:43 | ||||
| chr21:44339209-44339469 | Common:2; Rare:80 | ||||
| chr21:44873506-44873565 | Rare:16 | ||||
| chr21:44873570-44874050 | Common:8; Rare:191 | ||||
| chr21:44958315-44958378 | Common:1; Rare:18 | ||||
| chr21:45074475-45074776 | Common:3; Rare:142 | ||||
| chr21:45287875-45288100 | Common:6; Rare:88 | ||||
| chr21:45981526-45981841 | Common:23; Rare:77; Clinvar (benign):2 | ||||
| chr21:45981845-45981946 | Rare:31; Clinvar:5; Clinvar (benign):1 | ||||
| chr21:46000593-46000759 | Common:8; Rare:56; Clinvar:1; Clinvar (benign):1 |