| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49460508-49460821 | Common:6; Rare:222; Clinvar:13; Clinvar (benign):3 | ||||
| chr18:49487056-49487462 | Common:10; Rare:341 | ||||
| chr18:49491712-49491971 | Common:3; Rare:204 | ||||
| chr18:49492230-49492572 | Common:3; Rare:219 | ||||
| chr18:49561849-49562125 | Rare:118 | ||||
| chr18:49813497-49813641 | Rare:83 | ||||
| chr18:49813792-49814311 | Common:4; Rare:424 | ||||
| chr18:49849708-49850038 | Common:5; Rare:74 | ||||
| chr18:50194877-50195460 | Common:6; Rare:441; Clinvar:13; Clinvar (benign):1 | ||||
| chr18:50266310-50266870 | Common:1; Rare:172; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:50281411-50281927 | Common:9; Rare:449 | ||||
| chr18:50374827-50375173 | Common:8; Rare:194 | ||||
| chr18:50559820-50560190 | Common:5; Rare:109 | ||||
| chr18:50878775-50879259 | Common:13; Rare:337 | ||||
| chr18:50967845-50968094 | Rare:86 |