| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12991137-12991410 | Common:2; Rare:100 | ||||
| chr18:13726423-13726719 | Common:4; Rare:113 | ||||
| chr18:21111127-21111297 | Rare:36 | ||||
| chr18:21111307-21111356 | Common:1; Rare:14 | ||||
| chr18:21111522-21111923 | Common:2; Rare:123 | ||||
| chr18:21600454-21600791 | Rare:94 | ||||
| chr18:21600865-21600962 | Common:2; Rare:33 | ||||
| chr18:22913783-22914170 | Rare:66 | ||||
| chr18:22933235-22933454 | Common:3; Rare:80; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933807-22933903 | Common:1; Rare:38 | ||||
| chr18:23453172-23453469 | Rare:87 | ||||
| chr18:23503293-23503619 | Common:4; Rare:138 | ||||
| chr18:23586345-23586531 | Common:4; Rare:77; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23884349-23884677 | Common:1; Rare:57 | ||||
| chr18:24426620-24426785 | Common:3; Rare:64 |