| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37072698-37072742 | Rare:20 | ||||
| chr21:37072983-37073395 | Common:6; Rare:155 | ||||
| chr21:37267296-37267617 | Common:3; Rare:109 | ||||
| chr21:37267910-37267969 | Rare:25 | ||||
| chr21:37268080-37268191 | Common:3; Rare:28 | ||||
| chr21:37365995-37366121 | Rare:42 | ||||
| chr21:38296476-38296612 | Common:1; Rare:18 | ||||
| chr21:38498419-38498729 | Common:1; Rare:40 | ||||
| chr21:39387650-39387807 | Common:2; Rare:69 | ||||
| chr21:39445751-39445913 | Common:3; Rare:53 | ||||
| chr21:42879532-42879674 | Common:3; Rare:44 | ||||
| chr21:42893066-42893378 | Common:4; Rare:112 | ||||
| chr21:43659468-43659614 | Common:1; Rare:48 | ||||
| chr21:43733577-43733693 | Rare:22 | ||||
| chr21:43776204-43776665 | Common:5; Rare:158; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 |