| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47930694-47930884 | Rare:67 | ||||
| chr18:47931002-47931411 | Common:2; Rare:152 | ||||
| chr18:47931485-47931620 | Rare:41 | ||||
| chr18:48538894-48539060 | Rare:41 | ||||
| chr18:48948574-48948642 | Rare:20 | ||||
| chr18:48948689-48948896 | Rare:62 | ||||
| chr18:48949287-48949549 | Common:2; Rare:69 | ||||
| chr18:48949861-48950125 | Rare:85 | ||||
| chr18:48951031-48951178 | Common:3; Rare:17 | ||||
| chr18:49459886-49460222 | Common:7; Rare:96 | ||||
| chr18:49460508-49460872 | Common:2; Rare:105; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:49486797-49487041 | Rare:53 | ||||
| chr18:49487045-49487474 | Common:4; Rare:172 | ||||
| chr18:49491827-49491993 | Rare:53 | ||||
| chr18:49492372-49492521 | Rare:70 |