| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41508052-41508329 | Common:2; Rare:62 | ||||
| chr21:41766982-41767183 | Common:5; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr21:41879280-41879577 | Common:5; Rare:92 | ||||
| chr21:42010337-42010483 | Common:2; Rare:40 | ||||
| chr21:42315291-42315684 | Common:1; Rare:130 | ||||
| chr21:42496173-42496551 | Common:2; Rare:95; Clinvar:1 | ||||
| chr21:42514227-42514271 | Rare:10 | ||||
| chr21:42514421-42514663 | Rare:44 | ||||
| chr21:42731722-42732183 | Common:3; Rare:148 | ||||
| chr21:42756425-42756661 | Common:1; Rare:52 | ||||
| chr21:42756802-42757032 | Common:2; Rare:51 | ||||
| chr21:42893064-42893365 | Common:4; Rare:106 | ||||
| chr21:43659486-43659631 | Common:1; Rare:44 | ||||
| chr21:43776247-43776372 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr21:44089343-44089525 | Rare:51 |