| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10701402-10701463 | Rare:26 | ||||
| chr19:10836305-10836552 | Common:2; Rare:60 | ||||
| chr19:10928578-10928792 | Common:1; Rare:55 | ||||
| chr19:10960697-10961077 | Common:3; Rare:149 | ||||
| chr19:11089275-11089533 | Rare:46; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:11197498-11197633 | Common:1; Rare:35 | ||||
| chr19:11435168-11435443 | Common:2; Rare:72 | ||||
| chr19:11529086-11529287 | Rare:39 | ||||
| chr19:11559198-11559374 | Common:1; Rare:57 | ||||
| chr19:12551452-12551726 | Common:2; Rare:71 | ||||
| chr19:12610723-12610989 | Rare:91 | ||||
| chr19:12666704-12666864 | Rare:64; Clinvar:2 | ||||
| chr19:12681799-12682067 | Common:4; Rare:114 | ||||
| chr19:12696613-12696690 | Rare:35 | ||||
| chr19:12722623-12722843 | Common:1; Rare:46 |