| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:76491021-76491152 | Rare:36 | ||||
| chr18:76494776-76494934 | Common:1; Rare:38 | ||||
| chr18:76495186-76495696 | Common:4; Rare:126 | ||||
| chr18:76822173-76822405 | Common:10; Rare:68 | ||||
| chr18:76822454-76823011 | Common:4; Rare:188 | ||||
| chr18:77132071-77132342 | Common:3; Rare:73 | ||||
| chr18:77132744-77132918 | Rare:57 | ||||
| chr18:79068932-79069528 | Common:11; Rare:250 | ||||
| chr18:79069606-79069774 | Common:2; Rare:50 | ||||
| chr18:79343743-79344091 | Common:3; Rare:73 | ||||
| chr18:79395794-79395940 | Rare:33 | ||||
| chr18:79400232-79400331 | Common:2; Rare:37 | ||||
| chr18:79679316-79679500 | Rare:86 | ||||
| chr18:79679697-79679885 | Common:2; Rare:58 | ||||
| chr18:79680116-79680211 | Common:3; Rare:45; Clinvar (benign):3 |