| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019297-29019421 | Common:5; Rare:53 | ||||
| chr21:29024520-29024719 | Common:2; Rare:82 | ||||
| chr21:29073571-29073885 | Common:2; Rare:100 | ||||
| chr21:29298734-29298935 | Common:1; Rare:86 | ||||
| chr21:29300285-29300421 | Rare:38 | ||||
| chr21:31659360-31659837 | Common:2; Rare:193; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279040-32279214 | Common:3; Rare:71 | ||||
| chr21:32612544-32612631 | Rare:21 | ||||
| chr21:33266264-33266413 | Rare:44; Clinvar:3 | ||||
| chr21:33324854-33325058 | Common:4; Rare:88 | ||||
| chr21:33479859-33480136 | Rare:97 | ||||
| chr21:33542080-33542227 | Rare:58 | ||||
| chr21:33542805-33543165 | Common:3; Rare:122 | ||||
| chr21:33641712-33641980 | Common:1; Rare:69 | ||||
| chr21:36060508-36060583 | Common:1; Rare:21 |