| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42879422-42879716 | Common:6; Rare:188 | ||||
| chr21:42892999-42893356 | Common:10; Rare:243 | ||||
| chr21:42974107-42974594 | Common:2; Rare:297 | ||||
| chr21:42974930-42975229 | Common:7; Rare:145 | ||||
| chr21:43659418-43659636 | Common:2; Rare:123 | ||||
| chr21:43718972-43719523 | Common:13; Rare:260 | ||||
| chr21:43728440-43728790 | Common:5; Rare:156 | ||||
| chr21:43776243-43776676 | Common:10; Rare:295; Clinvar:4; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr21:43789341-43789638 | Common:2; Rare:214 | ||||
| chr21:43865048-43865324 | Common:1; Rare:95 | ||||
| chr21:44012133-44012407 | Common:4; Rare:195 | ||||
| chr21:44012620-44013080 | Rare:185 | ||||
| chr21:44299951-44300127 | Common:2; Rare:121; Clinvar (benign):1 | ||||
| chr21:44339226-44339493 | Common:5; Rare:146 | ||||
| chr21:44425560-44425846 | Common:4; Rare:222 |