| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46917883-46917922 | Rare:8 | ||||
| chr18:46946611-46946886 | Common:3; Rare:70 | ||||
| chr18:47150425-47150584 | Common:4; Rare:63 | ||||
| chr18:47930255-47930755 | Common:2; Rare:212 | ||||
| chr18:47930772-47930905 | Rare:50 | ||||
| chr18:47931047-47931274 | Rare:78 | ||||
| chr18:48538998-48539305 | Common:2; Rare:66 | ||||
| chr18:49460594-49460778 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49491707-49491943 | Common:1; Rare:77 | ||||
| chr18:49492224-49492588 | Common:2; Rare:140 | ||||
| chr18:49560457-49560756 | Common:6; Rare:61 | ||||
| chr18:49561896-49562097 | Rare:49 | ||||
| chr18:49813470-49814168 | Common:2; Rare:223 | ||||
| chr18:50280848-50281179 | Common:1; Rare:73 | ||||
| chr18:50281703-50281897 | Rare:68 |