| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:56651088-56651472 | Common:6; Rare:105 | ||||
| chr18:56651597-56651716 | Common:4; Rare:32 | ||||
| chr18:57586555-57586888 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr18:57621670-57622079 | Common:3; Rare:142 | ||||
| chr18:57622139-57622369 | Common:3; Rare:37 | ||||
| chr18:58044615-58044817 | Common:3; Rare:74 | ||||
| chr18:58091289-58091504 | Common:1; Rare:49 | ||||
| chr18:58195298-58195431 | Common:1; Rare:27 | ||||
| chr18:58536640-58536939 | Common:3; Rare:88 | ||||
| chr18:58670962-58671637 | Common:5; Rare:243; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58671957-58672091 | Rare:38 | ||||
| chr18:58863574-58863739 | Common:1; Rare:51 | ||||
| chr18:58864022-58864099 | Common:1; Rare:30 | ||||
| chr18:58964143-58964367 | Rare:44 | ||||
| chr18:59139363-59139518 | Rare:34 |