| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:21303244-21303410 | Rare:63 | ||||
| chr20:23350595-23350861 | Common:1; Rare:90 | ||||
| chr20:23421428-23421679 | Common:4; Rare:97 | ||||
| chr20:24992658-24992889 | Common:7; Rare:109 | ||||
| chr20:25247775-25248118 | Common:1; Rare:109 | ||||
| chr20:25407584-25407737 | Common:1; Rare:50 | ||||
| chr20:25623952-25624140 | Common:1; Rare:63 | ||||
| chr20:25696780-25697062 | Common:3; Rare:82 | ||||
| chr20:31722522-31722708 | Rare:38 | ||||
| chr20:31739136-31739355 | Common:1; Rare:55 | ||||
| chr20:32207676-32207939 | Common:3; Rare:97 | ||||
| chr20:33401482-33401649 | Rare:47 | ||||
| chr20:33731987-33732017 | Rare:15 | ||||
| chr20:34112102-34112423 | Rare:104 | ||||
| chr20:34303339-34303492 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 |