| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46098214-46098558 | Common:11; Rare:104; Clinvar (benign):6 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:46917390-46917659 | Common:2; Rare:114 | ||||
| chr18:47150414-47150584 | Common:4; Rare:65 | ||||
| chr18:49487075-49487355 | Common:4; Rare:105 | ||||
| chr18:49561879-49562100 | Rare:57 | ||||
| chr18:49813469-49813627 | Rare:38 | ||||
| chr18:49813821-49814206 | Common:1; Rare:159 | ||||
| chr18:50281436-50281835 | Common:3; Rare:124 | ||||
| chr18:50374941-50375083 | Rare:44 | ||||
| chr18:50878963-50879228 | Common:4; Rare:88 | ||||
| chr18:51030064-51030233 | Rare:54 | ||||
| chr18:54269492-54269612 | Common:1; Rare:63 | ||||
| chr18:55589725-55589996 | Common:2; Rare:88 | ||||
| chr18:56651178-56651414 | Common:4; Rare:63 |