| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49560838-49560904 | Rare:16 | ||||
| chr18:49560943-49561009 | Common:1; Rare:17 | ||||
| chr18:49561853-49562131 | Rare:73 | ||||
| chr18:49812269-49812573 | Common:1; Rare:57 | ||||
| chr18:49813122-49813188 | Rare:14 | ||||
| chr18:49813472-49813648 | Rare:42 | ||||
| chr18:49813802-49814115 | Common:1; Rare:126 | ||||
| chr18:49814381-49814467 | Rare:30 | ||||
| chr18:50194878-50195124 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):1 | ||||
| chr18:50266442-50266592 | Rare:60 | ||||
| chr18:50281450-50281625 | Common:2; Rare:60 | ||||
| chr18:50281671-50281914 | Common:1; Rare:78 | ||||
| chr18:50287623-50287829 | Rare:73 | ||||
| chr18:50287907-50288153 | Common:3; Rare:45 | ||||
| chr18:50288297-50288353 | Rare:11 |