| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46098233-46098550 | Common:11; Rare:91; Clinvar (benign):6 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917376-46917659 | Common:3; Rare:119 | ||||
| chr18:47150452-47150597 | Common:3; Rare:58 | ||||
| chr18:48538998-48539292 | Common:2; Rare:64 | ||||
| chr18:48539947-48539978 | Rare:4 | ||||
| chr18:49490452-49490930 | Common:1; Rare:118 | ||||
| chr18:49813826-49814303 | Common:2; Rare:194 | ||||
| chr18:50281453-50281821 | Common:3; Rare:112 | ||||
| chr18:50878954-50879235 | Common:4; Rare:95 | ||||
| chr18:51030054-51030227 | Rare:57 | ||||
| chr18:55321713-55321966 | Rare:57 | ||||
| chr18:55401678-55402003 | Rare:60 | ||||
| chr18:55588609-55588653 | Rare:8 | ||||
| chr18:55589713-55590004 | Common:2; Rare:97 |