| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29077398-29077524 | Rare:24 | ||||
| chr21:29298620-29298951 | Common:3; Rare:133 | ||||
| chr21:29300503-29300810 | Common:1; Rare:66 | ||||
| chr21:31559007-31559354 | Common:3; Rare:112 | ||||
| chr21:31659446-31659835 | Common:2; Rare:165; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732056-31732300 | Common:4; Rare:107 | ||||
| chr21:32278797-32278836 | Rare:19 | ||||
| chr21:32278975-32279214 | Common:3; Rare:110 | ||||
| chr21:32392878-32393187 | Common:3; Rare:129 | ||||
| chr21:32411624-32411811 | Rare:44 | ||||
| chr21:32585408-32585564 | Common:1; Rare:24 | ||||
| chr21:32612067-32612452 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr21:32612522-32612895 | Rare:92 | ||||
| chr21:32727905-32728158 | Rare:121; Clinvar:2 | ||||
| chr21:32771702-32772237 | Common:14; Rare:229 |