| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129197-36129471 | Common:4; Rare:80 | ||||
| chr18:36129776-36129934 | Common:1; Rare:63 | ||||
| chr18:36828719-36829141 | Common:3; Rare:157 | ||||
| chr18:45967261-45967449 | Rare:68 | ||||
| chr18:46098230-46098377 | Common:11; Rare:65; Clinvar (benign):6 | ||||
| chr18:46104136-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150452-47150524 | Common:2; Rare:28 | ||||
| chr18:49487174-49487328 | Common:2; Rare:58 | ||||
| chr18:49490452-49490915 | Common:1; Rare:114 | ||||
| chr18:49813826-49814138 | Common:1; Rare:130 | ||||
| chr18:50374876-50375137 | Common:3; Rare:85 | ||||
| chr18:50878954-50879219 | Common:4; Rare:90 | ||||
| chr18:50967912-50968070 | Rare:55 | ||||
| chr18:51030074-51030222 | Rare:46 | ||||
| chr18:54357860-54357977 | Common:6; Rare:35 |