| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41859665-41859984 | Common:1; Rare:91; Clinvar:1 | ||||
| chr19:41860078-41860731 | Common:7; Rare:227; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41883140-41883271 | Common:1; Rare:27 | ||||
| chr19:41884133-41884464 | Rare:86 | ||||
| chr19:41959157-41959456 | Common:1; Rare:114 | ||||
| chr19:42075707-42076296 | Common:5; Rare:170 | ||||
| chr19:42220111-42220358 | Common:2; Rare:66 | ||||
| chr19:42233224-42233326 | Rare:26 | ||||
| chr19:42242518-42242742 | Rare:67 | ||||
| chr19:42254998-42255191 | Common:1; Rare:68 | ||||
| chr19:42268262-42268576 | Rare:65 | ||||
| chr19:42301944-42302145 | Rare:51 | ||||
| chr19:42302232-42302818 | Common:1; Rare:153 | ||||
| chr19:43205616-43205668 | Common:4; Rare:13 | ||||
| chr19:43504014-43504397 | Common:7; Rare:121 |