| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34365066-34365251 | Common:1; Rare:79 | ||||
| chr19:34428319-34428502 | Rare:73 | ||||
| chr19:34677595-34677806 | Common:4; Rare:55 | ||||
| chr19:34733787-34734285 | Common:3; Rare:142 | ||||
| chr19:34926823-34927089 | Common:1; Rare:83 | ||||
| chr19:35000209-35000475 | Common:4; Rare:67 | ||||
| chr19:35030387-35030745 | Rare:114; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:35138648-35138873 | Rare:57 | ||||
| chr19:35139008-35139176 | Common:2; Rare:36 | ||||
| chr19:35139521-35139638 | Rare:27 | ||||
| chr19:35139679-35140062 | Common:5; Rare:92 | ||||
| chr19:35155148-35155230 | Rare:16 | ||||
| chr19:35268955-35269153 | Common:1; Rare:26 | ||||
| chr19:35545460-35545698 | Common:4; Rare:77 | ||||
| chr19:35628732-35629113 | Common:4; Rare:116 |