| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46714037-46714117 | Rare:21 | ||||
| chr19:46714274-46714789 | Common:4; Rare:105 | ||||
| chr19:46717024-46717517 | Common:4; Rare:128 | ||||
| chr19:46745830-46746103 | Common:3; Rare:67; Clinvar (benign):2 | ||||
| chr19:46746379-46746561 | Common:3; Rare:68 | ||||
| chr19:46786803-46786872 | Rare:13 | ||||
| chr19:46787492-46787694 | Rare:62 | ||||
| chr19:46788468-46788877 | Common:2; Rare:92 | ||||
| chr19:46850265-46850434 | Rare:24 | ||||
| chr19:46850771-46850898 | Rare:33 | ||||
| chr19:47035899-47036142 | Rare:88 | ||||
| chr19:47048181-47048316 | Common:1; Rare:42 | ||||
| chr19:47048544-47048917 | Common:1; Rare:121 | ||||
| chr19:47093950-47094075 | Rare:37 | ||||
| chr19:47112133-47112417 | Rare:86 |