| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35290178-35290391 | Common:2; Rare:76 | ||||
| chr18:35344376-35344687 | Common:2; Rare:101 | ||||
| chr18:35972345-35972759 | Common:4; Rare:142 | ||||
| chr18:36067425-36067716 | Common:2; Rare:103 | ||||
| chr18:36129203-36129466 | Common:4; Rare:79 | ||||
| chr18:36129812-36129951 | Rare:61 | ||||
| chr18:36828736-36829141 | Common:3; Rare:155 | ||||
| chr18:46098170-46098558 | Common:11; Rare:124; Clinvar (benign):8 | ||||
| chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr18:46173430-46173607 | Rare:47 | ||||
| chr18:47150437-47150526 | Common:2; Rare:36 | ||||
| chr18:48538994-48539302 | Common:2; Rare:68 | ||||
| chr18:48942522-48942872 | Common:2; Rare:100 | ||||
| chr18:49460599-49460832 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49561879-49562132 | Rare:62 |