| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36054388-36054579 | Common:3; Rare:54 | ||||
| chr19:36054705-36054971 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr19:36114801-36114989 | Common:2; Rare:80 | ||||
| chr19:36115680-36115795 | Rare:29 | ||||
| chr19:36139832-36140148 | Rare:95 | ||||
| chr19:36214639-36214747 | Common:1; Rare:32 | ||||
| chr19:36215055-36215196 | Rare:42 | ||||
| chr19:36379165-36379302 | Common:1; Rare:60 | ||||
| chr19:36418587-36418712 | Common:1; Rare:46 | ||||
| chr19:36489424-36489633 | Common:3; Rare:42 | ||||
| chr19:36528230-36528444 | Common:1; Rare:51 | ||||
| chr19:36528645-36528813 | Common:4; Rare:54 | ||||
| chr19:36573199-36573481 | Common:3; Rare:94 | ||||
| chr19:36666792-36666984 | Rare:54 | ||||
| chr19:36687366-36687655 | Common:3; Rare:99 |