| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:57661360-57661745 | Common:17; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:57669941-57669961 | |||||
| chr18:57679968-57680044 | Rare:11 | ||||
| chr18:57684300-57684378 | Common:1; Rare:11 | ||||
| chr18:57697804-57697944 | Rare:29; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr18:57738870-57738956 | Rare:10 | ||||
| chr18:57757290-57757321 | Rare:3 | ||||
| chr18:57764407-57764726 | Common:3; Rare:46 | ||||
| chr18:57766809-57766819 | Rare:2 | ||||
| chr18:57773929-57774034 | Rare:19 | ||||
| chr18:57777175-57777443 | Rare:51 | ||||
| chr18:57778727-57778965 | Rare:31 | ||||
| chr18:57790684-57790862 | Common:1; Rare:18 | ||||
| chr18:57793357-57793622 | Common:2; Rare:44 | ||||
| chr18:57794946-57795013 | Rare:14 |