| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:25561838-25562129 | Common:1; Rare:82 | ||||
| chr21:26964435-26964741 | Common:3; Rare:58 | ||||
| chr21:26967053-26967151 | Rare:24 | ||||
| chr21:26967903-26967947 | Rare:9 | ||||
| chr21:28048160-28048450 | Common:2; Rare:51 | ||||
| chr21:28114990-28115270 | Common:2; Rare:45 | ||||
| chr21:29002719-29002826 | Common:1; Rare:38 | ||||
| chr21:37221316-37221422 | Common:1; Rare:44 | ||||
| chr21:38907264-38907475 | Rare:39 | ||||
| chr21:38913562-38913687 | Common:5; Rare:27 | ||||
| chr21:42812774-42812824 | Common:1; Rare:10 | ||||
| chr21:44311146-44311290 | Common:3; Rare:52 | ||||
| chr21:45488193-45488448 | Common:3; Rare:75; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:45982506-45982757 | Rare:72; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:45992008-45992182 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 |