| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:56651133-56651705 | Common:9; Rare:141 | ||||
| chr18:57586589-57586793 | Rare:58 | ||||
| chr18:57621706-57621949 | Common:3; Rare:85 | ||||
| chr18:57803018-57803320 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:57803331-57803452 | Common:1; Rare:30 | ||||
| chr18:57803542-57803584 | Common:1; Rare:9 | ||||
| chr18:58045588-58045721 | Rare:36 | ||||
| chr18:58195514-58195662 | Common:1; Rare:60 | ||||
| chr18:58221392-58221629 | Common:2; Rare:44 | ||||
| chr18:58864804-58864885 | Rare:16 | ||||
| chr18:59139714-59140035 | Common:3; Rare:85 | ||||
| chr18:59359084-59359437 | Common:4; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:59697643-59697852 | Common:1; Rare:57 | ||||
| chr18:62186928-62187524 | Common:7; Rare:163 | ||||
| chr18:62522820-62523098 | Common:4; Rare:95 |