| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42010337-42010507 | Common:2; Rare:52 | ||||
| chr21:42315292-42315692 | Common:1; Rare:131 | ||||
| chr21:42496200-42496558 | Common:2; Rare:88 | ||||
| chr21:42514420-42514568 | Rare:30 | ||||
| chr21:42731562-42732151 | Common:3; Rare:169 | ||||
| chr21:42879527-42879665 | Common:3; Rare:46 | ||||
| chr21:42893064-42893354 | Common:4; Rare:100 | ||||
| chr21:43659468-43659667 | Common:1; Rare:66 | ||||
| chr21:43719013-43719358 | Common:6; Rare:113 | ||||
| chr21:43776258-43776657 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr21:43789369-43789617 | Common:1; Rare:89 | ||||
| chr21:44089318-44089497 | Rare:41 | ||||
| chr21:44089614-44089812 | Common:2; Rare:47 | ||||
| chr21:44299963-44300123 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr21:44300544-44300761 | Common:2; Rare:62 |