| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129812-36129962 | Rare:67 | ||||
| chr18:36187433-36187564 | Common:4; Rare:51 | ||||
| chr18:36828736-36829145 | Common:3; Rare:156 | ||||
| chr18:45967261-45967503 | Rare:89 | ||||
| chr18:46098235-46098365 | Common:5; Rare:55; Clinvar (benign):6 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:47150444-47150570 | Common:3; Rare:46 | ||||
| chr18:49487159-49487361 | Common:3; Rare:80 | ||||
| chr18:49813826-49814312 | Common:2; Rare:194 | ||||
| chr18:50878984-50879235 | Common:4; Rare:81 | ||||
| chr18:51030064-51030238 | Rare:57 | ||||
| chr18:54828605-54828674 | Common:1; Rare:10 | ||||
| chr18:54959389-54959509 | Common:1; Rare:35 | ||||
| chr18:55589723-55589996 | Common:2; Rare:88 | ||||
| chr18:56651133-56651554 | Common:5; Rare:104 |