| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600633-21600852 | Rare:52 | ||||
| chr18:21612174-21612441 | Common:1; Rare:79 | ||||
| chr18:22933240-22933426 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933814-22933909 | Common:1; Rare:34 | ||||
| chr18:23453126-23453353 | Rare:82 | ||||
| chr18:23586396-23586541 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24397768-24398073 | Common:2; Rare:114 | ||||
| chr18:24426613-24426763 | Common:3; Rare:61 | ||||
| chr18:26091128-26091491 | Common:2; Rare:82 | ||||
| chr18:32092388-32092706 | Common:4; Rare:142 | ||||
| chr18:35041244-35041471 | Common:1; Rare:85 | ||||
| chr18:35240917-35241109 | Common:2; Rare:71 | ||||
| chr18:35290188-35290384 | Common:2; Rare:69 | ||||
| chr18:35344394-35344606 | Common:2; Rare:72 | ||||
| chr18:35972478-35972722 | Common:3; Rare:77 |