| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:45967261-45967503 | Rare:89 | ||||
| chr18:46098045-46098355 | Common:6; Rare:126; Clinvar (benign):8 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150435-47150557 | Common:3; Rare:47 | ||||
| chr18:48538998-48539287 | Common:2; Rare:62 | ||||
| chr18:49487079-49487335 | Common:3; Rare:94 | ||||
| chr18:49490452-49490914 | Common:1; Rare:114 | ||||
| chr18:49561879-49562071 | Rare:50 | ||||
| chr18:49813815-49814206 | Common:1; Rare:159 | ||||
| chr18:50274997-50275157 | Rare:53 | ||||
| chr18:50879011-50879228 | Common:4; Rare:73 | ||||
| chr18:51030064-51030222 | Rare:51 | ||||
| chr18:54357872-54357924 | Rare:13 | ||||
| chr18:55321754-55322018 | Common:1; Rare:61 | ||||
| chr18:55401664-55401711 | Rare:8 |