| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26845405-26845555 | Common:1; Rare:36 | ||||
| chr21:28885337-28885426 | Common:2; Rare:69 | ||||
| chr21:28992763-28993169 | Common:2; Rare:160 | ||||
| chr21:29019297-29019467 | Common:5; Rare:74 | ||||
| chr21:29024530-29024738 | Common:2; Rare:93 | ||||
| chr21:29024869-29025043 | Rare:32 | ||||
| chr21:29073571-29073870 | Common:2; Rare:91 | ||||
| chr21:29298638-29298951 | Common:3; Rare:126 | ||||
| chr21:31558979-31559333 | Common:3; Rare:112 | ||||
| chr21:31659491-31659838 | Common:2; Rare:156; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732069-31732332 | Common:4; Rare:122 | ||||
| chr21:32278970-32279214 | Common:3; Rare:112 | ||||
| chr21:32392892-32393205 | Common:4; Rare:131 | ||||
| chr21:32612305-32612910 | Common:1; Rare:146 | ||||
| chr21:32727889-32728183 | Rare:139; Clinvar:2 |