| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26170585-26170926 | Common:5; Rare:108; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26843071-26843141 | Common:3; Rare:10 | ||||
| chr21:28992797-28993130 | Common:2; Rare:138 | ||||
| chr21:29019287-29019414 | Common:5; Rare:51 | ||||
| chr21:29024537-29024776 | Common:2; Rare:103 | ||||
| chr21:29073562-29073769 | Common:2; Rare:70 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279011-32279174 | Common:2; Rare:75 | ||||
| chr21:32392906-32393191 | Common:4; Rare:120 | ||||
| chr21:32612522-32612872 | Rare:85 | ||||
| chr21:32727897-32728120 | Rare:109; Clinvar:2 | ||||
| chr21:32771715-32772171 | Common:13; Rare:200 | ||||
| chr21:33229763-33229938 | Common:3; Rare:72 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324866-33325111 | Common:4; Rare:106 |