| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43659468-43659592 | Common:1; Rare:43 | ||||
| chr21:43776208-43776642 | Common:5; Rare:149; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789363-43789617 | Common:1; Rare:91 | ||||
| chr21:44425567-44425735 | Common:1; Rare:67 | ||||
| chr21:44872590-44872690 | Rare:24 | ||||
| chr21:44873503-44873565 | Rare:16 | ||||
| chr21:44873570-44874061 | Common:9; Rare:192 | ||||
| chr21:44939892-44940060 | Common:2; Rare:50 | ||||
| chr21:45287857-45288093 | Common:6; Rare:95 | ||||
| chr21:45404934-45405241 | Common:13; Rare:173 | ||||
| chr21:45981531-45981848 | Common:24; Rare:80; Clinvar (benign):3 | ||||
| chr21:46184404-46184756 | Common:4; Rare:32 | ||||
| chr21:46286266-46286370 | Common:2; Rare:38 | ||||
| chr21:46323823-46324222 | Common:3; Rare:146; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458686-46459063 | Common:3; Rare:130 |