| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:8609282-8609558 | Common:2; Rare:102 | ||||
| chr18:8704801-8705394 | Common:3; Rare:177 | ||||
| chr18:8705414-8705611 | Rare:46 | ||||
| chr18:9102429-9102779 | Common:2; Rare:145; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9103132-9103212 | Common:1; Rare:18 | ||||
| chr18:9135940-9136276 | Common:6; Rare:102 | ||||
| chr18:9136277-9136888 | Rare:202 | ||||
| chr18:9136985-9137089 | Common:1; Rare:35 | ||||
| chr18:9137167-9137584 | Common:4; Rare:148 | ||||
| chr18:9334376-9334911 | Common:1; Rare:129 | ||||
| chr18:9334917-9334984 | Rare:18 | ||||
| chr18:9474781-9475084 | Common:2; Rare:70 | ||||
| chr18:9475101-9475741 | Common:10; Rare:173 | ||||
| chr18:9475777-9475967 | Common:2; Rare:57 | ||||
| chr18:9476219-9476396 | Common:1; Rare:38 |