| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586360-23586563 | Common:4; Rare:87; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23872688-23873047 | Rare:88; Clinvar (pathogenic):1 | ||||
| chr18:24397712-24397978 | Common:2; Rare:97 | ||||
| chr18:24426657-24426786 | Common:2; Rare:54 | ||||
| chr18:25351033-25351133 | Rare:35 | ||||
| chr18:25352072-25352410 | Common:2; Rare:135 | ||||
| chr18:26090499-26090709 | Common:1; Rare:97 | ||||
| chr18:26546972-26547046 | Rare:23 | ||||
| chr18:28176995-28177295 | Common:3; Rare:143 | ||||
| chr18:31102300-31102603 | Rare:74; Clinvar:4 | ||||
| chr18:31498062-31498326 | Common:1; Rare:97; Clinvar:8; Clinvar (benign):7 | ||||
| chr18:31943087-31943418 | Common:7; Rare:110 | ||||
| chr18:32018374-32018903 | Common:4; Rare:146 | ||||
| chr18:32091853-32091991 | Common:3; Rare:51 | ||||
| chr18:32092384-32092738 | Common:5; Rare:159 |