| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23689296-23689763 | Common:1; Rare:169 | ||||
| chr18:23992560-23992880 | Common:1; Rare:62 | ||||
| chr18:24014306-24014453 | Common:1; Rare:33 | ||||
| chr18:24014525-24014841 | Common:6; Rare:164 | ||||
| chr18:24397666-24398013 | Common:3; Rare:187 | ||||
| chr18:24426575-24426834 | Common:7; Rare:173 | ||||
| chr18:26090562-26090902 | Common:8; Rare:255 | ||||
| chr18:26091141-26091371 | Common:3; Rare:76 | ||||
| chr18:26226244-26226587 | Common:8; Rare:206 | ||||
| chr18:26548760-26549010 | Rare:60 | ||||
| chr18:26549110-26549243 | Rare:48 | ||||
| chr18:26549710-26550110 | Common:10; Rare:184 | ||||
| chr18:26657343-26657877 | Common:1; Rare:153 | ||||
| chr18:31498063-31498279 | Common:2; Rare:148; Clinvar:10; Clinvar (benign):12 | ||||
| chr18:31684970-31685700 | Common:11; Rare:284 |