| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:25734851-25735485 | Common:5; Rare:218 | ||||
| chr21:25735584-25735779 | Common:1; Rare:47 | ||||
| chr21:26844267-26844531 | Common:3; Rare:108 | ||||
| chr21:26845323-26845503 | Common:1; Rare:51 | ||||
| chr21:28885336-28885415 | Common:2; Rare:62 | ||||
| chr21:29019297-29019430 | Common:5; Rare:56 | ||||
| chr21:29024619-29024726 | Common:1; Rare:45 | ||||
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073586-29073856 | Common:2; Rare:81 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279017-32279205 | Common:3; Rare:83 | ||||
| chr21:32298839-32298974 | Rare:47 | ||||
| chr21:32392955-32393172 | Common:2; Rare:92 | ||||
| chr21:32411591-32411768 | Rare:47 | ||||
| chr21:32412374-32412750 | Common:2; Rare:81 |