| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35972449-35972731 | Common:4; Rare:95 | ||||
| chr18:36129177-36129525 | Common:4; Rare:105 | ||||
| chr18:36129776-36129939 | Common:1; Rare:67 | ||||
| chr18:36828748-36829132 | Common:3; Rare:143 | ||||
| chr18:45967281-45967465 | Rare:65 | ||||
| chr18:46098244-46098581 | Common:11; Rare:92; Clinvar (benign):5 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150445-47150558 | Common:3; Rare:42 | ||||
| chr18:49460626-49460930 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487174-49487317 | Common:2; Rare:52 | ||||
| chr18:49490452-49490915 | Common:1; Rare:114 | ||||
| chr18:49561879-49562104 | Rare:58 | ||||
| chr18:49813862-49814068 | Common:1; Rare:96 | ||||
| chr18:50281432-50281573 | Rare:52 | ||||
| chr18:50281754-50281837 | Rare:27 |