| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50281423-50281584 | Common:1; Rare:58 | ||||
| chr18:50878966-50879228 | Common:4; Rare:87 | ||||
| chr18:51030064-51030222 | Rare:51 | ||||
| chr18:54357790-54357990 | Common:8; Rare:65 | ||||
| chr18:55401657-55401882 | Rare:42 | ||||
| chr18:55589707-55589908 | Rare:54 | ||||
| chr18:56651133-56651376 | Common:3; Rare:62 | ||||
| chr18:57621730-57621969 | Common:3; Rare:87 | ||||
| chr18:57803345-57803454 | Common:1; Rare:30 | ||||
| chr18:59139732-59139964 | Common:2; Rare:64 | ||||
| chr18:62186974-62187328 | Common:5; Rare:99 | ||||
| chr18:63367138-63367369 | Common:1; Rare:85 | ||||
| chr18:63422352-63422665 | Common:1; Rare:87 | ||||
| chr18:68714987-68715216 | Common:3; Rare:99 | ||||
| chr18:70205659-70205803 | Common:3; Rare:59; Clinvar (benign):2 |