| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019297-29019454 | Common:10; Rare:135 | ||||
| chr21:29024422-29024726 | Common:6; Rare:196 | ||||
| chr21:29024810-29025130 | Common:2; Rare:117 | ||||
| chr21:29073568-29073870 | Common:4; Rare:171 | ||||
| chr21:29298714-29298947 | Common:4; Rare:195 | ||||
| chr21:29299142-29299445 | Common:4; Rare:180 | ||||
| chr21:31659491-31659842 | Common:4; Rare:270; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr21:31731884-31732291 | Common:8; Rare:296 | ||||
| chr21:31872907-31873672 | Common:10; Rare:330 | ||||
| chr21:32278995-32279214 | Common:6; Rare:185 | ||||
| chr21:32392893-32393197 | Common:6; Rare:230 | ||||
| chr21:32612544-32612950 | Rare:193 | ||||
| chr21:32727899-32728168 | Rare:241; Clinvar:4 | ||||
| chr21:32771681-32772237 | Common:27; Rare:460 | ||||
| chr21:33229824-33230037 | Common:8; Rare:99 |