| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26843555-26843713 | Common:2; Rare:36 | ||||
| chr21:26845362-26845643 | Common:3; Rare:110 | ||||
| chr21:28885306-28885431 | Common:3; Rare:91 | ||||
| chr21:28992795-28993110 | Common:4; Rare:253 | ||||
| chr21:29019166-29019469 | Common:11; Rare:188 | ||||
| chr21:29024500-29024751 | Common:6; Rare:191 | ||||
| chr21:29024770-29025160 | Common:2; Rare:117 | ||||
| chr21:29073567-29073884 | Common:4; Rare:191 | ||||
| chr21:29076750-29077121 | Common:4; Rare:162 | ||||
| chr21:29077286-29077486 | Rare:48 | ||||
| chr21:29298590-29298954 | Common:3; Rare:219 | ||||
| chr21:29299046-29299612 | Common:2; Rare:216 | ||||
| chr21:31659502-31659837 | Common:4; Rare:234; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr21:31731889-31732298 | Common:8; Rare:307 | ||||
| chr21:32278989-32279214 | Common:6; Rare:199 |