| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9117765-9117903 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:9119254-9119561 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr18:9136492-9136964 | Rare:177 | ||||
| chr18:9137080-9137354 | Common:3; Rare:108 | ||||
| chr18:9334463-9334920 | Common:1; Rare:110 | ||||
| chr18:9474816-9475077 | Common:1; Rare:65 | ||||
| chr18:9615030-9615174 | Common:1; Rare:39 | ||||
| chr18:9615186-9615374 | Common:1; Rare:29 | ||||
| chr18:9708040-9708419 | Common:5; Rare:101 | ||||
| chr18:9913719-9914103 | Common:1; Rare:135 | ||||
| chr18:9914185-9914331 | Rare:62 | ||||
| chr18:10455086-10455149 | Common:1; Rare:21 | ||||
| chr18:10525849-10526132 | Common:2; Rare:109 | ||||
| chr18:11851246-11851878 | Common:3; Rare:217 | ||||
| chr18:11908224-11908456 | Rare:69 |