| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801707-44801890 | Rare:70 | ||||
| chr21:44873503-44873565 | Rare:16 | ||||
| chr21:44873612-44874050 | Common:8; Rare:177 | ||||
| chr21:44939870-44940060 | Common:2; Rare:54 | ||||
| chr21:45073782-45073845 | Common:2; Rare:27 | ||||
| chr21:45287857-45288102 | Common:6; Rare:98 | ||||
| chr21:45404928-45405233 | Common:13; Rare:177 | ||||
| chr21:45505232-45505390 | Common:4; Rare:91; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr21:45981505-45981822 | Common:23; Rare:74; Clinvar (benign):2 | ||||
| chr21:46184392-46184741 | Common:4; Rare:34 | ||||
| chr21:46286233-46286407 | Common:4; Rare:66 | ||||
| chr21:46323780-46324202 | Common:2; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46324462-46324663 | Common:4; Rare:76 | ||||
| chr21:46458682-46459012 | Common:3; Rare:113 | ||||
| chr21:46635480-46635737 | Common:5; Rare:83 |