| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43659485-43659609 | Common:1; Rare:36 | ||||
| chr21:44012167-44012523 | Common:2; Rare:132 | ||||
| chr21:44299974-44300136 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr21:44801707-44801890 | Rare:70 | ||||
| chr21:44873607-44874057 | Common:9; Rare:178 | ||||
| chr21:44939877-44940116 | Common:2; Rare:65 | ||||
| chr21:45073779-45073840 | Common:2; Rare:24 | ||||
| chr21:45287879-45288129 | Common:5; Rare:93 | ||||
| chr21:45404899-45405222 | Common:13; Rare:181 | ||||
| chr21:45405473-45405694 | Rare:64 | ||||
| chr21:45981490-45981808 | Common:23; Rare:72; Clinvar (benign):2 | ||||
| chr21:46286226-46286436 | Common:4; Rare:81 | ||||
| chr21:46286460-46286708 | Common:1; Rare:78 | ||||
| chr21:46323801-46324202 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46458686-46459057 | Common:3; Rare:127 |