| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51196195-51196618 | Rare:125 | ||||
| chr18:51196640-51196760 | Rare:43 | ||||
| chr18:54224457-54224845 | Common:1; Rare:103 | ||||
| chr18:54269398-54269714 | Common:5; Rare:127 | ||||
| chr18:54269742-54270116 | Common:2; Rare:100 | ||||
| chr18:54357580-54358026 | Common:10; Rare:125 | ||||
| chr18:54358589-54358645 | Rare:18 | ||||
| chr18:55321566-55321569 | |||||
| chr18:55321679-55321966 | Rare:66 | ||||
| chr18:55322314-55322707 | Common:1; Rare:76 | ||||
| chr18:55322721-55322784 | Rare:11 | ||||
| chr18:55511028-55511115 | Rare:18 | ||||
| chr18:55588094-55588148 | Rare:17; Clinvar (benign):1 | ||||
| chr18:55589775-55590064 | Common:2; Rare:99 | ||||
| chr18:56638498-56638998 | Common:8; Rare:163 |