| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:25352092-25352410 | Common:2; Rare:129 | ||||
| chr18:26090554-26090703 | Common:1; Rare:74 | ||||
| chr18:26548892-26549211 | Rare:84 | ||||
| chr18:31042480-31042883 | Common:1; Rare:108 | ||||
| chr18:31101682-31102186 | Common:2; Rare:102; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102194-31102451 | Common:1; Rare:59; Clinvar:7 | ||||
| chr18:31317932-31318257 | Common:1; Rare:51 | ||||
| chr18:31447583-31447980 | Common:4; Rare:83 | ||||
| chr18:31497995-31498259 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:31943095-31943400 | Common:7; Rare:102 | ||||
| chr18:32092388-32092747 | Common:5; Rare:160 | ||||
| chr18:34976921-34977061 | Common:1; Rare:24 | ||||
| chr18:35240917-35241094 | Common:2; Rare:66 | ||||
| chr18:35290158-35290391 | Common:2; Rare:77 | ||||
| chr18:35344376-35344515 | Common:2; Rare:46 |