| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:16573308-16573540 | Common:1; Rare:63 | ||||
| chr20:17569227-17569334 | Rare:18 | ||||
| chr20:17968438-17968594 | Common:4; Rare:65 | ||||
| chr20:17968784-17968935 | Common:1; Rare:65 | ||||
| chr20:18467137-18467448 | Common:1; Rare:64 | ||||
| chr20:18507792-18507952 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:23086265-23086450 | Rare:35 | ||||
| chr20:23350549-23350830 | Common:1; Rare:87 | ||||
| chr20:25623956-25624140 | Common:1; Rare:60 | ||||
| chr20:25696766-25697091 | Common:3; Rare:92 | ||||
| chr20:31547278-31547438 | Rare:40 | ||||
| chr20:31739101-31739369 | Common:1; Rare:69 | ||||
| chr20:32207683-32207939 | Common:3; Rare:95 | ||||
| chr20:33401481-33401618 | Rare:34 | ||||
| chr20:34303277-34303380 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 |