| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45322819-45323119 | Common:2; Rare:58 | ||||
| chr19:45370544-45370829 | Common:2; Rare:87 | ||||
| chr19:45406334-45406680 | Common:2; Rare:84 | ||||
| chr19:45423477-45423676 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr19:45423839-45423952 | Common:2; Rare:31 | ||||
| chr19:45506862-45506969 | Rare:30 | ||||
| chr19:45507400-45507516 | Rare:35 | ||||
| chr19:45584764-45585008 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45639362-45639459 | Common:1; Rare:29 | ||||
| chr19:45667944-45668257 | Common:2; Rare:54 | ||||
| chr19:45692523-45692742 | Common:1; Rare:60 | ||||
| chr19:45730868-45731073 | Common:1; Rare:45 | ||||
| chr19:45769186-45769355 | Rare:54 | ||||
| chr19:45769375-45769712 | Common:3; Rare:151 | ||||
| chr19:45863108-45863421 | Common:4; Rare:100 |