| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32483475-32483690 | Rare:40 | ||||
| chr20:33401476-33401618 | Rare:37 | ||||
| chr20:33720205-33720500 | Common:4; Rare:77 | ||||
| chr20:33993906-33994125 | Rare:88 | ||||
| chr20:34112094-34112452 | Rare:118 | ||||
| chr20:34302959-34303165 | Rare:63 | ||||
| chr20:34303274-34303393 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:34363182-34363325 | Rare:38 | ||||
| chr20:34516312-34516451 | Common:3; Rare:55 | ||||
| chr20:34516641-34516712 | Rare:30 | ||||
| chr20:34677054-34677318 | Rare:74 | ||||
| chr20:34825483-34825793 | Rare:115 | ||||
| chr20:34872811-34872944 | Rare:46 | ||||
| chr20:34876239-34876617 | Common:3; Rare:101 | ||||
| chr20:34955689-34955868 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):3 |