| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404825-45405231 | Common:13; Rare:207 | ||||
| chr21:45542374-45542545 | Rare:61 | ||||
| chr21:45981455-45981818 | Common:23; Rare:86; Clinvar (benign):2 | ||||
| chr21:45981847-45981950 | Rare:33; Clinvar:5; Clinvar (benign):1 | ||||
| chr21:45982220-45982359 | Common:7; Rare:31 | ||||
| chr21:45987146-45987200 | Rare:21; Clinvar:2 | ||||
| chr21:45987491-45987657 | Rare:72; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:45999136-45999340 | Common:1; Rare:73; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45999660-46000120 | Common:34; Rare:161; Clinvar:2; Clinvar (benign):3 | ||||
| chr21:46097295-46097630 | Common:3; Rare:67 | ||||
| chr21:46097643-46098182 | Common:7; Rare:160; Clinvar (benign):1 | ||||
| chr21:46098391-46098794 | Common:4; Rare:105 | ||||
| chr21:46113309-46113624 | Common:1; Rare:71 | ||||
| chr21:46113995-46114134 | Common:1; Rare:43; Clinvar:5; Clinvar (benign):1 | ||||
| chr21:46228742-46228916 | Common:3; Rare:85 |