| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29073579-29073870 | Common:2; Rare:87 | ||||
| chr21:29298600-29298930 | Common:2; Rare:126 | ||||
| chr21:31659502-31659824 | Common:2; Rare:147; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr21:31732069-31732335 | Common:4; Rare:124 | ||||
| chr21:32278985-32279214 | Common:3; Rare:102 | ||||
| chr21:32392906-32393163 | Common:2; Rare:107 | ||||
| chr21:32612309-32612651 | Common:1; Rare:83 | ||||
| chr21:32771746-32772237 | Common:14; Rare:210 | ||||
| chr21:33266255-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324844-33325068 | Common:4; Rare:91 | ||||
| chr21:33403290-33403534 | Common:1; Rare:60 | ||||
| chr21:33479908-33480198 | Common:1; Rare:90 | ||||
| chr21:33542080-33542248 | Rare:67 | ||||
| chr21:33542805-33543090 | Common:3; Rare:104 | ||||
| chr21:33641718-33641944 | Common:1; Rare:55 |