| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42496188-42496586 | Common:2; Rare:98 | ||||
| chr21:42514424-42514556 | Rare:28 | ||||
| chr21:42653007-42653151 | Rare:28 | ||||
| chr21:42653507-42653813 | Common:5; Rare:52 | ||||
| chr21:42879532-42879680 | Common:3; Rare:44 | ||||
| chr21:42893004-42893351 | Common:5; Rare:120 | ||||
| chr21:43659441-43659638 | Common:1; Rare:63 | ||||
| chr21:43728603-43728900 | Common:3; Rare:75 | ||||
| chr21:43740800-43741029 | Common:4; Rare:76 | ||||
| chr21:43776231-43776493 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789408-43789638 | Common:1; Rare:93 | ||||
| chr21:44299992-44300132 | Rare:53; Clinvar (benign):1 | ||||
| chr21:44339203-44339469 | Common:2; Rare:83 | ||||
| chr21:44455280-44455610 | Common:5; Rare:77 | ||||
| chr21:44455812-44455845 | Rare:7 |