| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11089300-11089528 | Rare:42; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11197504-11197633 | Common:1; Rare:35 | ||||
| chr19:11203408-11203760 | Rare:85 | ||||
| chr19:11339589-11339808 | Common:3; Rare:60 | ||||
| chr19:11435158-11435440 | Common:2; Rare:72 | ||||
| chr19:11446987-11447101 | Rare:41 | ||||
| chr19:11538623-11538999 | Common:4; Rare:88 | ||||
| chr19:11546676-11546969 | Rare:81 | ||||
| chr19:11559195-11559374 | Common:1; Rare:59 | ||||
| chr19:11738881-11739203 | Common:4; Rare:92 | ||||
| chr19:11924969-11925170 | Common:6; Rare:67 | ||||
| chr19:12140335-12140452 | Rare:35 | ||||
| chr19:12484737-12484964 | Common:1; Rare:57 | ||||
| chr19:12551421-12551690 | Common:2; Rare:75 | ||||
| chr19:12610688-12610994 | Rare:99 |