| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024867-29025048 | Rare:34 | ||||
| chr21:29073592-29073865 | Common:2; Rare:80 | ||||
| chr21:29298728-29298947 | Common:2; Rare:95 | ||||
| chr21:31659537-31659838 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732054-31732300 | Common:4; Rare:110 | ||||
| chr21:32278970-32279214 | Common:3; Rare:112 | ||||
| chr21:32392897-32393147 | Common:2; Rare:103 | ||||
| chr21:32612507-32612910 | Rare:100 | ||||
| chr21:32727897-32728133 | Rare:117; Clinvar:2 | ||||
| chr21:32771707-32772243 | Common:14; Rare:227 | ||||
| chr21:33266262-33266458 | Rare:64; Clinvar:3 | ||||
| chr21:33324854-33325098 | Common:4; Rare:107 | ||||
| chr21:33479854-33480204 | Common:1; Rare:112 | ||||
| chr21:33491675-33491856 | Common:2; Rare:49 | ||||
| chr21:33542080-33542235 | Rare:61 |