| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39451596-39451949 | Common:1; Rare:80 | ||||
| chr21:41316676-41316891 | Rare:48 | ||||
| chr21:41361913-41362039 | Common:1; Rare:17 | ||||
| chr21:41420209-41420333 | Common:2; Rare:36 | ||||
| chr21:41426032-41426312 | Common:3; Rare:63 | ||||
| chr21:41508052-41508314 | Common:2; Rare:58 | ||||
| chr21:41766998-41767167 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr21:41879295-41879529 | Common:5; Rare:77 | ||||
| chr21:42403680-42403934 | Common:1; Rare:52 | ||||
| chr21:42514441-42514556 | Rare:25 | ||||
| chr21:42879522-42879674 | Common:3; Rare:51 | ||||
| chr21:42893053-42893361 | Common:4; Rare:108 | ||||
| chr21:43659486-43659592 | Common:1; Rare:33 | ||||
| chr21:43719037-43719359 | Common:6; Rare:109 | ||||
| chr21:43775962-43776483 | Common:7; Rare:161; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 |