| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39348905-39349452 | Common:19; Rare:171 | ||||
| chr21:39380207-39380493 | Common:1; Rare:133 | ||||
| chr21:39387625-39387781 | Common:2; Rare:65 | ||||
| chr21:39445751-39445925 | Common:3; Rare:56 | ||||
| chr21:41879329-41879608 | Common:5; Rare:86 | ||||
| chr21:42010306-42010507 | Common:2; Rare:64 | ||||
| chr21:42496200-42496621 | Common:2; Rare:104 | ||||
| chr21:42513608-42513905 | Rare:87 | ||||
| chr21:42514382-42514542 | Rare:35 | ||||
| chr21:42653450-42653817 | Common:5; Rare:56 | ||||
| chr21:42879491-42879680 | Common:3; Rare:75 | ||||
| chr21:42892986-42893361 | Common:5; Rare:131 | ||||
| chr21:42974242-42974652 | Common:1; Rare:151 | ||||
| chr21:43659448-43659644 | Common:1; Rare:64 | ||||
| chr21:43776223-43776611 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):2 |