| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44071943-44072166 | Common:1; Rare:54 | ||||
| chr19:44113181-44113443 | Common:3; Rare:58 | ||||
| chr19:44141472-44141643 | Common:2; Rare:23 | ||||
| chr19:44164925-44165142 | Common:1; Rare:54 | ||||
| chr19:44212330-44212594 | Common:4; Rare:78 | ||||
| chr19:44305001-44305162 | Rare:42 | ||||
| chr19:44500483-44500649 | Common:3; Rare:50 | ||||
| chr19:44643798-44644036 | Rare:59 | ||||
| chr19:45038937-45039094 | Rare:53 | ||||
| chr19:45405045-45405175 | Rare:30 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45423477-45423710 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr19:45507228-45507717 | Common:1; Rare:128 | ||||
| chr19:46346951-46347137 | Common:3; Rare:56 | ||||
| chr19:46413552-46413773 | Common:1; Rare:70 |