| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44745592-44746520 | Common:14; Rare:539 | ||||
| chr20:44885253-44885814 | Common:27; Rare:530 | ||||
| chr20:44885851-44886251 | Rare:211 | ||||
| chr20:44909911-44910141 | Common:6; Rare:287 | ||||
| chr20:44910072-44910918 | Common:9; Rare:411 | ||||
| chr20:44960271-44960671 | Common:6; Rare:535 | ||||
| chr20:44965968-44966648 | Common:9; Rare:725 | ||||
| chr20:45347840-45348281 | Common:11; Rare:157 | ||||
| chr20:45348370-45348730 | Common:2; Rare:127 | ||||
| chr20:45362813-45363273 | Common:6; Rare:782 | ||||
| chr20:45363243-45363728 | Common:14; Rare:543 | ||||
| chr20:45406083-45406760 | Common:5; Rare:538 | ||||
| chr20:45406670-45406970 | Rare:70 | ||||
| chr20:45415820-45416214 | Common:2; Rare:453; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr20:45416226-45416626 | Rare:144; Clinvar (pathogenic):2 |