| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46364391-46364553 | Rare:63 | ||||
| chr20:46406571-46406787 | Common:2; Rare:57 | ||||
| chr20:49219211-49219464 | Common:1; Rare:114 | ||||
| chr20:49278037-49278291 | Rare:71 | ||||
| chr20:50113112-50113241 | Common:5; Rare:62 | ||||
| chr20:50794854-50795027 | Common:1; Rare:59 | ||||
| chr20:50958478-50958834 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:56392187-56392687 | Common:6; Rare:129 | ||||
| chr20:56468331-56468699 | Rare:122 | ||||
| chr20:58651113-58651305 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58840342-58840753 | Common:1; Rare:156; Clinvar:3 | ||||
| chr20:58852815-58853068 | Common:1; Rare:54 | ||||
| chr20:58854168-58854342 | Rare:75; Clinvar:2 | ||||
| chr20:58909950-58910370 | Rare:98 | ||||
| chr20:59940247-59940481 | Rare:94 |