| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12947662-12948061 | Common:3; Rare:104 | ||||
| chr18:12991143-12991405 | Common:2; Rare:97 | ||||
| chr18:13218684-13218808 | Common:1; Rare:23 | ||||
| chr18:13726445-13726724 | Common:3; Rare:108 | ||||
| chr18:21111651-21111985 | Common:2; Rare:115 | ||||
| chr18:21600655-21600931 | Common:2; Rare:74 | ||||
| chr18:22169345-22169608 | Common:1; Rare:68 | ||||
| chr18:23453113-23453345 | Rare:83 | ||||
| chr18:23586373-23586537 | Common:3; Rare:71; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:24426620-24426749 | Common:3; Rare:55 | ||||
| chr18:32092367-32092694 | Common:4; Rare:148 | ||||
| chr18:34593206-34593365 | Rare:36 | ||||
| chr18:34976942-34977067 | Common:1; Rare:22 | ||||
| chr18:35041247-35041467 | Common:1; Rare:83 | ||||
| chr18:35240917-35241094 | Common:2; Rare:66 |