| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:32569740-32570003 | Common:4; Rare:66 | ||||
| chr21:32632377-32632385 | Rare:4 | ||||
| chr21:32738624-32738932 | Common:2; Rare:58 | ||||
| chr21:32741534-32741755 | Common:1; Rare:45 | ||||
| chr21:32758090-32758311 | Common:1; Rare:36 | ||||
| chr21:32758540-32758639 | Rare:8 | ||||
| chr21:32765890-32766120 | Common:1; Rare:43 | ||||
| chr21:33232666-33233119 | Rare:76 | ||||
| chr21:33233373-33233681 | Common:2; Rare:50 | ||||
| chr21:33242482-33242730 | Common:5; Rare:33 | ||||
| chr21:33421366-33421537 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:33548208-33548288 | Rare:17 | ||||
| chr21:33559205-33559795 | Common:1; Rare:116 | ||||
| chr21:33570346-33570560 | Rare:43 | ||||
| chr21:33575019-33575350 | Common:1; Rare:82 |