| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38850786-38850851 | Common:1; Rare:11 | ||||
| chr19:38850936-38850954 | Rare:5 | ||||
| chr19:38851869-38852121 | Common:2; Rare:94 | ||||
| chr19:38852305-38852498 | Rare:50 | ||||
| chr19:38852622-38852745 | Common:1; Rare:31 | ||||
| chr19:38869781-38870203 | Common:3; Rare:125 | ||||
| chr19:38899481-38900108 | Rare:179 | ||||
| chr19:38900169-38900318 | Common:1; Rare:30 | ||||
| chr19:38912154-38912377 | Common:1; Rare:67 | ||||
| chr19:38930303-38930581 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:38930661-38931197 | Common:6; Rare:154; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:38949694-38950033 | Common:2; Rare:111 | ||||
| chr19:38974890-38975215 | Rare:47 | ||||
| chr19:38975240-38975414 | Common:1; Rare:28 | ||||
| chr19:38975440-38975522 | Rare:17 |