| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:28770428-28770688 | Common:1; Rare:48 | ||||
| chr21:28770870-28771160 | Common:1; Rare:45 | ||||
| chr21:28772018-28772247 | Common:2; Rare:36 | ||||
| chr21:29002719-29002861 | Common:2; Rare:52 | ||||
| chr21:32569488-32569638 | Rare:30 | ||||
| chr21:36135556-36135597 | Rare:5 | ||||
| chr21:37221316-37221444 | Common:1; Rare:54 | ||||
| chr21:38503632-38503861 | Common:1; Rare:45 | ||||
| chr21:42534634-42534717 | Rare:14 | ||||
| chr21:44989376-44989814 | Common:7; Rare:91 | ||||
| chr21:44991792-44992126 | Common:7; Rare:71 | ||||
| chr21:45041348-45041603 | Common:2; Rare:50 | ||||
| chr21:45984033-45984452 | Common:4; Rare:126; Clinvar:17; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr21:45997422-45997761 | Common:5; Rare:115; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr21:45998132-45998416 | Common:1; Rare:97; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 |