| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:24992661-24992839 | Common:5; Rare:81 | ||||
| chr20:25195617-25195848 | Common:4; Rare:76 | ||||
| chr20:25247794-25248362 | Common:2; Rare:197 | ||||
| chr20:25623956-25624157 | Common:1; Rare:69 | ||||
| chr20:25696752-25697066 | Common:3; Rare:90 | ||||
| chr20:31547278-31547438 | Rare:40 | ||||
| chr20:31722481-31722660 | Rare:36 | ||||
| chr20:31722699-31722963 | Rare:63 | ||||
| chr20:31723527-31723715 | Common:1; Rare:51 | ||||
| chr20:32207703-32207939 | Common:3; Rare:91 | ||||
| chr20:33401489-33401589 | Rare:25 | ||||
| chr20:33993073-33993285 | Rare:58 | ||||
| chr20:34112119-34112583 | Common:1; Rare:145 | ||||
| chr20:34303281-34303320 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr20:34516331-34516443 | Rare:41 |