| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55589710-55590069 | Common:2; Rare:114 | ||||
| chr18:56637893-56637991 | Common:2; Rare:19 | ||||
| chr18:56638153-56638280 | Rare:26 | ||||
| chr18:56638353-56638403 | Rare:16 | ||||
| chr18:56638516-56638979 | Common:8; Rare:156 | ||||
| chr18:56651093-56651509 | Common:6; Rare:109 | ||||
| chr18:57435137-57435418 | Rare:79 | ||||
| chr18:57586364-57586407 | Common:1; Rare:6 | ||||
| chr18:57586424-57586652 | Common:1; Rare:75 | ||||
| chr18:57586655-57586918 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr18:57587206-57587228 | Rare:4 | ||||
| chr18:57621353-57621371 | Rare:5 | ||||
| chr18:57621644-57622033 | Common:6; Rare:135 | ||||
| chr18:57622149-57622231 | Common:1; Rare:21 | ||||
| chr18:57803270-57803480 | Common:2; Rare:55 |