| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54959389-54959561 | Common:2; Rare:47 | ||||
| chr18:55589744-55589906 | Rare:45 | ||||
| chr18:56651133-56651379 | Common:3; Rare:62 | ||||
| chr18:58221398-58221622 | Common:2; Rare:40 | ||||
| chr18:62186937-62187328 | Common:5; Rare:108 | ||||
| chr18:63422375-63422708 | Common:2; Rare:95 | ||||
| chr18:68714960-68715250 | Common:6; Rare:130 | ||||
| chr18:70205659-70205750 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr18:74499776-74499917 | Common:2; Rare:30 | ||||
| chr18:74597583-74597889 | Common:2; Rare:83 | ||||
| chr18:75209073-75209240 | Common:1; Rare:60 | ||||
| chr18:77087462-77087535 | Common:3; Rare:19 | ||||
| chr18:79988356-79988661 | Common:4; Rare:110; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572237-572637 | Common:3; Rare:199 | ||||
| chr19:633520-633749 | Common:8; Rare:100 |