| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46173713-46174140 | Common:3; Rare:100 | ||||
| chr18:46917354-46917659 | Common:3; Rare:135 | ||||
| chr18:46946528-46946850 | Common:3; Rare:74 | ||||
| chr18:47150450-47150570 | Common:3; Rare:43 | ||||
| chr18:48137041-48137231 | Common:1; Rare:36 | ||||
| chr18:48949379-48949545 | Common:1; Rare:50 | ||||
| chr18:48951165-48951418 | Common:1; Rare:46 | ||||
| chr18:49487161-49487317 | Common:2; Rare:57 | ||||
| chr18:49813476-49813627 | Rare:36 | ||||
| chr18:49813826-49814312 | Common:2; Rare:194 | ||||
| chr18:50274990-50275157 | Rare:54 | ||||
| chr18:50281754-50281908 | Rare:61 | ||||
| chr18:50374876-50375083 | Common:2; Rare:72 | ||||
| chr18:50878948-50879228 | Common:4; Rare:94 |