| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55322596-55322667 | Rare:13 | ||||
| chr18:55322692-55322784 | Rare:12 | ||||
| chr18:55400784-55400815 | Rare:6 | ||||
| chr18:55400856-55401141 | Rare:58 | ||||
| chr18:55401379-55401386 | Rare:1 | ||||
| chr18:55401644-55401822 | Rare:34 | ||||
| chr18:55401969-55402118 | Common:1; Rare:26 | ||||
| chr18:55402174-55402197 | Rare:3 | ||||
| chr18:55422168-55422308 | Rare:28 | ||||
| chr18:55510721-55510781 | Rare:10 | ||||
| chr18:55510935-55511030 | Rare:21 | ||||
| chr18:55511034-55511129 | Rare:21 | ||||
| chr18:55587515-55587942 | Rare:95 | ||||
| chr18:55588074-55588518 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:55588548-55588621 | Rare:18 |