| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36060470-36060583 | Common:2; Rare:33 | ||||
| chr21:36134917-36135087 | Rare:44 | ||||
| chr21:36320068-36320267 | Common:3; Rare:101 | ||||
| chr21:37073040-37073390 | Common:5; Rare:132 | ||||
| chr21:37267290-37267673 | Common:4; Rare:137 | ||||
| chr21:38498442-38498595 | Rare:17 | ||||
| chr21:38805588-38805659 | Rare:17 | ||||
| chr21:38805794-38806060 | Common:2; Rare:68 | ||||
| chr21:39183381-39183543 | Common:3; Rare:69 | ||||
| chr21:41508079-41508272 | Common:2; Rare:42 | ||||
| chr21:41767024-41767173 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:42893088-42893336 | Common:3; Rare:81 | ||||
| chr21:43775976-43776374 | Common:4; Rare:119; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789375-43789659 | Common:1; Rare:105 | ||||
| chr21:44801740-44801870 | Rare:61 |