| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36319965-36320261 | Common:4; Rare:143 | ||||
| chr21:37072595-37072665 | Common:1; Rare:36 | ||||
| chr21:37072979-37073373 | Common:6; Rare:152 | ||||
| chr21:37267304-37267719 | Common:4; Rare:147 | ||||
| chr21:38256872-38257192 | Common:1; Rare:62 | ||||
| chr21:39380385-39380416 | Rare:15 | ||||
| chr21:39387650-39387813 | Common:2; Rare:72 | ||||
| chr21:39445751-39445883 | Common:3; Rare:40 | ||||
| chr21:41767007-41767176 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:41879320-41879565 | Common:5; Rare:79 | ||||
| chr21:42514390-42514545 | Rare:34 | ||||
| chr21:42893073-42893347 | Common:3; Rare:96 | ||||
| chr21:43659468-43659585 | Common:1; Rare:40 | ||||
| chr21:43776204-43776385 | Common:2; Rare:67; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789369-43789638 | Common:1; Rare:100 |