| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35497880-35498029 | Common:1; Rare:50 | ||||
| chr18:35972478-35972750 | Common:3; Rare:96 | ||||
| chr18:36129144-36129471 | Common:4; Rare:96 | ||||
| chr18:36129782-36129962 | Common:1; Rare:77 | ||||
| chr18:36187388-36187534 | Common:2; Rare:53 | ||||
| chr18:36828715-36829148 | Common:3; Rare:160 | ||||
| chr18:45967235-45967503 | Rare:100; Clinvar (pathogenic):1 | ||||
| chr18:46098175-46098365 | Common:5; Rare:85; Clinvar (benign):8 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917341-46917652 | Common:3; Rare:135 | ||||
| chr18:47150420-47150567 | Common:4; Rare:55 | ||||
| chr18:48137041-48137241 | Common:1; Rare:38 | ||||
| chr18:49487089-49487379 | Common:4; Rare:111 | ||||
| chr18:49490452-49490920 | Common:1; Rare:114 | ||||
| chr18:49561911-49562081 | Rare:38 |