| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13726424-13726729 | Common:4; Rare:114 | ||||
| chr18:21600644-21600852 | Rare:49 | ||||
| chr18:21704662-21705001 | Common:3; Rare:106 | ||||
| chr18:22169345-22169589 | Common:1; Rare:64 | ||||
| chr18:22933272-22933426 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933779-22933903 | Common:1; Rare:50 | ||||
| chr18:23437887-23438047 | Common:2; Rare:71 | ||||
| chr18:23453156-23453379 | Rare:77 | ||||
| chr18:23503344-23503576 | Rare:88 | ||||
| chr18:23529827-23530115 | Common:3; Rare:63 | ||||
| chr18:23586387-23586546 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24426620-24426779 | Common:3; Rare:62 | ||||
| chr18:28176989-28177232 | Common:3; Rare:114 | ||||
| chr18:31101460-31101622 | Common:9; Rare:54 | ||||
| chr18:31498050-31498259 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):5 |