| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36135308-36135418 | Rare:39 | ||||
| chr21:36320162-36320584 | Common:5; Rare:167 | ||||
| chr21:36698982-36699168 | Common:2; Rare:53 | ||||
| chr21:36990208-36990279 | Common:3; Rare:28; Clinvar (benign):3 | ||||
| chr21:37072511-37072689 | Common:4; Rare:92; Clinvar (pathogenic):1 | ||||
| chr21:37072698-37072741 | Rare:19 | ||||
| chr21:37072989-37073379 | Common:5; Rare:151 | ||||
| chr21:37267296-37267704 | Common:4; Rare:144 | ||||
| chr21:37267910-37268028 | Rare:36 | ||||
| chr21:37366000-37366107 | Rare:35 | ||||
| chr21:38498403-38498686 | Common:1; Rare:35 | ||||
| chr21:38660557-38660813 | Common:1; Rare:63 | ||||
| chr21:38804923-38805186 | Common:2; Rare:68 | ||||
| chr21:38805724-38806093 | Common:2; Rare:96 | ||||
| chr21:39445748-39445925 | Common:3; Rare:57 |