| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23086199-23086498 | Common:1; Rare:69 | ||||
| chr20:24992702-24992885 | Common:6; Rare:89 | ||||
| chr20:25195598-25195865 | Common:4; Rare:80 | ||||
| chr20:25623952-25624027 | Common:1; Rare:34 | ||||
| chr20:25696769-25697091 | Common:3; Rare:92 | ||||
| chr20:31547294-31547438 | Rare:36 | ||||
| chr20:31605680-31605813 | Common:1; Rare:70 | ||||
| chr20:31722702-31722935 | Rare:57 | ||||
| chr20:32207676-32207958 | Common:3; Rare:109 | ||||
| chr20:33401481-33401607 | Rare:31 | ||||
| chr20:34516281-34516451 | Common:3; Rare:69 | ||||
| chr20:34558563-34558780 | Common:1; Rare:55 | ||||
| chr20:34677086-34677293 | Rare:54 | ||||
| chr20:34732579-34732863 | Common:1; Rare:48 | ||||
| chr20:34955733-34955817 | Common:1; Rare:33; Clinvar:3; Clinvar (benign):2 |