| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45769388-45769717 | Common:3; Rare:146 | ||||
| chr19:45792740-45793260 | Common:7; Rare:126 | ||||
| chr19:45862495-45862712 | Rare:56 | ||||
| chr19:45863096-45863423 | Common:4; Rare:105 | ||||
| chr19:45886090-45886201 | Rare:44 | ||||
| chr19:45886620-45887010 | Common:5; Rare:110 | ||||
| chr19:45902585-45902938 | Common:3; Rare:109 | ||||
| chr19:45973986-45974193 | Rare:44 | ||||
| chr19:46077432-46078051 | Common:5; Rare:136 | ||||
| chr19:46296792-46297086 | Common:4; Rare:118 | ||||
| chr19:46346794-46347143 | Common:3; Rare:114 | ||||
| chr19:46413424-46413768 | Common:1; Rare:100 | ||||
| chr19:46471482-46471676 | Common:5; Rare:77 | ||||
| chr19:46495862-46496054 | Rare:52 | ||||
| chr19:46600870-46601413 | Common:5; Rare:186; Clinvar (benign):1 |