| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32359173-32359401 | Rare:64 | ||||
| chr20:32535403-32535486 | Common:1; Rare:16 | ||||
| chr20:32536261-32536597 | Common:3; Rare:80 | ||||
| chr20:32743353-32743614 | Common:1; Rare:64 | ||||
| chr20:32743892-32744130 | Rare:36 | ||||
| chr20:32762126-32762441 | Common:2; Rare:108; Clinvar:1 | ||||
| chr20:32762496-32762657 | Rare:58; Clinvar:2 | ||||
| chr20:32819705-32820010 | Common:3; Rare:104 | ||||
| chr20:32820127-32820331 | Common:1; Rare:66 | ||||
| chr20:33401021-33401295 | Common:1; Rare:53 | ||||
| chr20:33401404-33401645 | Rare:69 | ||||
| chr20:33443858-33444016 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:33489773-33490175 | Common:3; Rare:146 | ||||
| chr20:33490399-33490534 | Rare:23 | ||||
| chr20:33663599-33664023 | Common:4; Rare:186 |