| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48538911-48539059 | Rare:36 | ||||
| chr18:48933161-48933316 | Rare:34 | ||||
| chr18:48948689-48948862 | Rare:49 | ||||
| chr18:48949331-48949563 | Common:2; Rare:69 | ||||
| chr18:48949914-48950030 | Rare:45 | ||||
| chr18:48951064-48951174 | Common:2; Rare:13 | ||||
| chr18:49459866-49460205 | Common:7; Rare:99 | ||||
| chr18:49460421-49460450 | Rare:9; Clinvar:1 | ||||
| chr18:49460583-49460872 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:49486808-49487032 | Rare:49 | ||||
| chr18:49487072-49487455 | Common:4; Rare:153 | ||||
| chr18:49491677-49491982 | Common:1; Rare:103 | ||||
| chr18:49492374-49492551 | Common:1; Rare:77 | ||||
| chr18:49561853-49562098 | Rare:67 | ||||
| chr18:49813401-49813728 | Common:2; Rare:76 |