| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29077374-29077483 | Rare:31 | ||||
| chr21:29077685-29077931 | Rare:61 | ||||
| chr21:29298515-29298985 | Common:3; Rare:174 | ||||
| chr21:29299153-29299409 | Common:1; Rare:78 | ||||
| chr21:29300253-29300421 | Rare:43 | ||||
| chr21:29300620-29300967 | Rare:73 | ||||
| chr21:31559963-31559999 | Common:1; Rare:14 | ||||
| chr21:31659482-31659807 | Common:2; Rare:147; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr21:31731898-31732412 | Common:5; Rare:211 | ||||
| chr21:31732420-31732494 | Common:1; Rare:24 | ||||
| chr21:31732497-31732625 | Common:1; Rare:32 | ||||
| chr21:32278969-32279243 | Common:3; Rare:122 | ||||
| chr21:32392940-32393277 | Common:5; Rare:132 | ||||
| chr21:32612319-32612980 | Rare:168 | ||||
| chr21:32727293-32727547 | Common:2; Rare:55 |