| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57351081-57351340 | Common:2; Rare:82 | ||||
| chr20:57351466-57351517 | Rare:21 | ||||
| chr20:57351627-57351740 | Rare:29 | ||||
| chr20:57391106-57391416 | Common:7; Rare:121 | ||||
| chr20:57391877-57392265 | Common:6; Rare:103 | ||||
| chr20:57620286-57620693 | Common:2; Rare:86 | ||||
| chr20:57710010-57710181 | Rare:53 | ||||
| chr20:58309333-58309842 | Common:4; Rare:209 | ||||
| chr20:58309997-58310229 | Common:1; Rare:60 | ||||
| chr20:58388953-58389357 | Common:4; Rare:197; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58389484-58389687 | Rare:66; Clinvar:1 | ||||
| chr20:58651002-58651374 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58652077-58652126 | Rare:14; Clinvar (benign):1 | ||||
| chr20:58652277-58652599 | Common:2; Rare:103 | ||||
| chr20:58692644-58692830 | Common:2; Rare:57 |