| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45507391-45507708 | Rare:90 | ||||
| chr19:45584760-45585054 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45642267-45642551 | Common:2; Rare:85 | ||||
| chr19:45692372-45692713 | Common:1; Rare:79 | ||||
| chr19:45768256-45768487 | Rare:101; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45769200-45769353 | Rare:52 | ||||
| chr19:46303495-46303630 | Common:1; Rare:19 | ||||
| chr19:46346938-46347210 | Common:3; Rare:94 | ||||
| chr19:46375385-46375663 | Common:2; Rare:67 | ||||
| chr19:46471207-46471366 | Common:3; Rare:31 | ||||
| chr19:46495838-46495966 | Rare:40 | ||||
| chr19:46600888-46601434 | Common:6; Rare:190; Clinvar (benign):3 | ||||
| chr19:46717075-46717263 | Common:2; Rare:65 | ||||
| chr19:46725348-46725597 | Rare:90 | ||||
| chr19:46728309-46728346 | Rare:10 |