| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019312-29019434 | Common:5; Rare:48 | ||||
| chr21:29073592-29073865 | Common:2; Rare:80 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279012-32279205 | Common:3; Rare:85 | ||||
| chr21:32392956-32393202 | Common:4; Rare:104 | ||||
| chr21:32612293-32612636 | Common:1; Rare:83 | ||||
| chr21:32727897-32728133 | Rare:117; Clinvar:2 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324866-33325058 | Common:4; Rare:83 | ||||
| chr21:33542080-33542232 | Rare:61 | ||||
| chr21:33542812-33543086 | Common:3; Rare:97 | ||||
| chr21:34526780-34527077 | Common:1; Rare:53 | ||||
| chr21:35049231-35049489 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:36060308-36060583 | Common:3; Rare:70 | ||||
| chr21:36319994-36320251 | Common:3; Rare:126 |