| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586394-23586537 | Common:2; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138900-24139069 | Common:2; Rare:53 | ||||
| chr18:24271632-24271733 | Common:2; Rare:28 | ||||
| chr18:24397758-24398091 | Common:2; Rare:119 | ||||
| chr18:25352104-25352438 | Common:2; Rare:133 | ||||
| chr18:26035580-26035637 | Rare:13 | ||||
| chr18:26091097-26091403 | Common:2; Rare:71 | ||||
| chr18:28177013-28177043 | Rare:13 | ||||
| chr18:28177079-28177272 | Common:3; Rare:85 | ||||
| chr18:28177432-28177457 | Rare:9 | ||||
| chr18:31942422-31942518 | Rare:29 | ||||
| chr18:31943084-31943322 | Common:1; Rare:68 | ||||
| chr18:32091609-32091888 | Common:6; Rare:66 | ||||
| chr18:32092356-32092754 | Common:6; Rare:182 | ||||
| chr18:34709176-34709347 | Rare:20 |