| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55588111-55588334 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:55589696-55589906 | Rare:59 | ||||
| chr18:56651133-56651388 | Common:3; Rare:63 | ||||
| chr18:57621724-57621964 | Common:3; Rare:87 | ||||
| chr18:58045582-58045747 | Rare:46 | ||||
| chr18:58864799-58864911 | Rare:18 | ||||
| chr18:59697377-59697682 | Common:1; Rare:96 | ||||
| chr18:59697689-59697852 | Common:1; Rare:43 | ||||
| chr18:62186960-62187320 | Common:5; Rare:100 | ||||
| chr18:63367115-63367328 | Common:1; Rare:74 | ||||
| chr18:63422370-63422716 | Common:2; Rare:103 | ||||
| chr18:68715030-68715287 | Common:5; Rare:110 | ||||
| chr18:70205659-70205784 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr18:72544316-72544530 | Common:1; Rare:62 | ||||
| chr18:74148352-74148552 | Common:1; Rare:65 |