| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33542081-33542191 | Rare:39 | ||||
| chr21:33542805-33543090 | Common:3; Rare:104 | ||||
| chr21:36319965-36320258 | Common:4; Rare:142 | ||||
| chr21:37072605-37072720 | Common:3; Rare:57 | ||||
| chr21:37073019-37073363 | Common:5; Rare:134 | ||||
| chr21:37267296-37267682 | Common:4; Rare:136 | ||||
| chr21:37365989-37366073 | Rare:28 | ||||
| chr21:38661757-38662038 | Rare:48 | ||||
| chr21:39445776-39445883 | Common:1; Rare:35 | ||||
| chr21:41767046-41767167 | Common:3; Rare:58; Clinvar:1 | ||||
| chr21:42974254-42974606 | Common:1; Rare:135 | ||||
| chr21:43659486-43659609 | Common:1; Rare:36 | ||||
| chr21:44873612-44874071 | Common:9; Rare:181 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 | ||||
| chr21:45981500-45981946 | Common:24; Rare:119; Clinvar:5; Clinvar (benign):4 |