| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32357595-32358529 | Common:6; Rare:233; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:32358826-32359009 | Common:3; Rare:70 | ||||
| chr20:32359389-32359398 | Rare:1 | ||||
| chr20:32743359-32743721 | Common:1; Rare:81 | ||||
| chr20:32743926-32744008 | Rare:13 | ||||
| chr20:32762043-32762461 | Common:3; Rare:132; Clinvar:1 | ||||
| chr20:32762537-32762624 | Rare:21; Clinvar:1 | ||||
| chr20:32819718-32820010 | Common:3; Rare:102 | ||||
| chr20:32820119-32820445 | Common:2; Rare:105 | ||||
| chr20:33401427-33401650 | Rare:65 | ||||
| chr20:33443879-33443990 | Rare:33; Clinvar:2 | ||||
| chr20:33489740-33490180 | Common:4; Rare:157 | ||||
| chr20:33663613-33664012 | Common:4; Rare:179 | ||||
| chr20:33666719-33667071 | Common:1; Rare:99 | ||||
| chr20:33674333-33674613 | Common:1; Rare:97 |