| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50878984-50879235 | Common:4; Rare:81 | ||||
| chr18:51030054-51030226 | Rare:56 | ||||
| chr18:54357882-54357903 | Rare:3 | ||||
| chr18:54959354-54959536 | Common:2; Rare:50 | ||||
| chr18:55321746-55321942 | Rare:45 | ||||
| chr18:55589769-55590004 | Common:2; Rare:84 | ||||
| chr18:56651133-56651554 | Common:5; Rare:104 | ||||
| chr18:56651615-56651708 | Common:3; Rare:24 | ||||
| chr18:62186987-62187320 | Common:5; Rare:95 | ||||
| chr18:62522816-62523055 | Common:4; Rare:80 | ||||
| chr18:63367105-63367328 | Common:1; Rare:78 | ||||
| chr18:63422352-63422646 | Common:1; Rare:78 | ||||
| chr18:67516691-67516785 | Common:1; Rare:27 | ||||
| chr18:68714977-68715262 | Common:6; Rare:126 | ||||
| chr18:70205648-70205783 | Common:3; Rare:56; Clinvar (benign):2 |