| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586354-23586528 | Common:4; Rare:73; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:31943109-31943375 | Common:7; Rare:87 | ||||
| chr18:32092387-32092694 | Common:4; Rare:135 | ||||
| chr18:34976934-34977067 | Common:1; Rare:24 | ||||
| chr18:35240917-35241094 | Common:2; Rare:66 | ||||
| chr18:35290193-35290377 | Common:2; Rare:67 | ||||
| chr18:35972449-35972739 | Common:4; Rare:98 | ||||
| chr18:36129223-36129545 | Common:4; Rare:107 | ||||
| chr18:36129772-36129936 | Common:1; Rare:66 | ||||
| chr18:36828765-36829141 | Common:3; Rare:138 | ||||
| chr18:45967261-45967487 | Rare:82 | ||||
| chr18:46098175-46098571 | Common:11; Rare:126; Clinvar (benign):8 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46756811-46756965 | Common:2; Rare:43 | ||||
| chr18:47150438-47150554 | Common:3; Rare:44 |