| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44011575-44012499 | Common:16; Rare:609 | ||||
| chr21:44012539-44013130 | Rare:763 | ||||
| chr21:44133250-44133700 | Common:6; Rare:78 | ||||
| chr21:44299386-44300151 | Common:8; Rare:582; Clinvar (benign):4 | ||||
| chr21:44300370-44300471 | Rare:24 | ||||
| chr21:44300437-44300880 | Common:6; Rare:271 | ||||
| chr21:44338212-44338612 | Common:4; Rare:210 | ||||
| chr21:44338732-44339170 | Common:17; Rare:151; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:44339190-44339640 | Common:21; Rare:539 | ||||
| chr21:44339624-44340148 | Common:8; Rare:167 | ||||
| chr21:44425440-44425869 | Common:10; Rare:715 | ||||
| chr21:44801630-44802030 | Common:5; Rare:584 | ||||
| chr21:44801974-44802713 | Common:13; Rare:358 | ||||
| chr21:44817604-44818004 | Common:19; Rare:223 | ||||
| chr21:44817957-44818324 | Common:3; Rare:521 |