| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54357878-54357971 | Common:4; Rare:23 | ||||
| chr18:55588120-55588294 | Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:55589722-55589906 | Rare:50 | ||||
| chr18:56651132-56651413 | Common:4; Rare:74 | ||||
| chr18:56651598-56651710 | Common:4; Rare:29 | ||||
| chr18:57586545-57586813 | Rare:81 | ||||
| chr18:57621707-57621975 | Common:3; Rare:93 | ||||
| chr18:59139727-59140033 | Common:3; Rare:83 | ||||
| chr18:62186915-62187363 | Common:6; Rare:124 | ||||
| chr18:63367099-63367357 | Common:1; Rare:95 | ||||
| chr18:63367543-63367627 | Common:2; Rare:31 | ||||
| chr18:63422375-63422669 | Common:1; Rare:82 | ||||
| chr18:68714977-68715317 | Common:7; Rare:140 | ||||
| chr18:69957142-69957309 | Rare:39 | ||||
| chr18:74148353-74148590 | Common:1; Rare:72 |