| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55587354-55588081 | Common:2; Rare:247; Clinvar:1; Clinvar (benign):3 | ||||
| chr18:55588078-55588633 | Common:3; Rare:410; Clinvar:12; Clinvar (benign):8 | ||||
| chr18:55588551-55588951 | Common:2; Rare:72 | ||||
| chr18:55589669-55590077 | Common:14; Rare:650 | ||||
| chr18:55590133-55590921 | Common:1; Rare:190 | ||||
| chr18:56638097-56638497 | Common:1; Rare:120 | ||||
| chr18:56638476-56638931 | Common:20; Rare:535 | ||||
| chr18:56649984-56650664 | Common:6; Rare:133 | ||||
| chr18:56651099-56651862 | Common:55; Rare:899 | ||||
| chr18:57435080-57435480 | Common:1; Rare:384 | ||||
| chr18:57586220-57587130 | Common:4; Rare:493; Clinvar (benign):2 | ||||
| chr18:57587071-57587545 | Rare:148 | ||||
| chr18:57620664-57621365 | Common:7; Rare:213 | ||||
| chr18:57621707-57622470 | Common:23; Rare:747 | ||||
| chr18:57622660-57623060 | Common:2; Rare:72 |