| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:28992797-28993060 | Common:1; Rare:115 | ||||
| chr21:29019307-29019421 | Common:5; Rare:49 | ||||
| chr21:29024508-29024776 | Common:3; Rare:107 | ||||
| chr21:29024858-29025013 | Rare:34 | ||||
| chr21:29073541-29073865 | Common:2; Rare:102 | ||||
| chr21:31659545-31659838 | Common:2; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32278992-32279219 | Common:3; Rare:100 | ||||
| chr21:32298442-32298681 | Rare:55 | ||||
| chr21:32298684-32299014 | Common:2; Rare:98; Clinvar (pathogenic):1 | ||||
| chr21:32392917-32393197 | Common:4; Rare:120 | ||||
| chr21:32411624-32411786 | Rare:40 | ||||
| chr21:32612305-32612886 | Common:1; Rare:141 | ||||
| chr21:32727889-32728168 | Rare:133; Clinvar:2 | ||||
| chr21:32771688-32772241 | Common:14; Rare:235 | ||||
| chr21:33266253-33266496 | Rare:73; Clinvar:3 |