| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37072511-37072726 | Common:5; Rare:111; Clinvar (pathogenic):1 | ||||
| chr21:37073003-37073469 | Common:5; Rare:164 | ||||
| chr21:37081307-37081332 | Rare:7 | ||||
| chr21:37108155-37108197 | Rare:5 | ||||
| chr21:37159476-37159742 | Common:1; Rare:56 | ||||
| chr21:37267278-37267692 | Common:4; Rare:152 | ||||
| chr21:37367011-37367072 | Common:1; Rare:20 | ||||
| chr21:38805787-38805938 | Common:1; Rare:34 | ||||
| chr21:39348466-39348694 | Common:4; Rare:104 | ||||
| chr21:39348904-39349164 | Common:1; Rare:94 | ||||
| chr21:39445736-39445922 | Common:3; Rare:61 | ||||
| chr21:41252295-41252499 | Common:1; Rare:41 | ||||
| chr21:42010268-42010518 | Common:2; Rare:81 | ||||
| chr21:42879516-42879656 | Common:3; Rare:53 | ||||
| chr21:42893022-42893378 | Common:4; Rare:131 |