| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49460588-49460804 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:49487122-49487316 | Common:3; Rare:71 | ||||
| chr18:49561879-49562071 | Rare:50 | ||||
| chr18:49813918-49814216 | Rare:125 | ||||
| chr18:50374909-50375080 | Common:1; Rare:58 | ||||
| chr18:50878984-50879228 | Common:4; Rare:79 | ||||
| chr18:51030060-51030222 | Rare:53 | ||||
| chr18:54357848-54357971 | Common:5; Rare:35 | ||||
| chr18:55321632-55321942 | Rare:69 | ||||
| chr18:55322334-55322577 | Rare:53 | ||||
| chr18:55401024-55401146 | Rare:22 | ||||
| chr18:55401341-55401739 | Common:4; Rare:79 | ||||
| chr18:55401754-55401814 | Rare:12 | ||||
| chr18:55422839-55423035 | Common:1; Rare:34 | ||||
| chr18:55585880-55585948 | Common:1; Rare:11 |