| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111625-21111953 | Common:2; Rare:107 | ||||
| chr18:21612234-21612441 | Common:1; Rare:66 | ||||
| chr18:22933791-22933889 | Common:1; Rare:38 | ||||
| chr18:23453156-23453340 | Rare:66 | ||||
| chr18:23586402-23586553 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138883-24139069 | Common:2; Rare:56 | ||||
| chr18:24397788-24397992 | Common:2; Rare:85 | ||||
| chr18:24426595-24426765 | Common:3; Rare:69 | ||||
| chr18:26090542-26090948 | Common:4; Rare:159 | ||||
| chr18:26091154-26091491 | Common:2; Rare:75 | ||||
| chr18:32092388-32092745 | Common:5; Rare:157 | ||||
| chr18:35240917-35241090 | Common:2; Rare:64 | ||||
| chr18:35290183-35290384 | Common:2; Rare:72 | ||||
| chr18:35344392-35344544 | Common:2; Rare:50 | ||||
| chr18:35972462-35972714 | Common:3; Rare:78 |