| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10180564-10180811 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:10251771-10252028 | Common:1; Rare:63 | ||||
| chr19:10315729-10316285 | Common:7; Rare:204; Clinvar (benign):13 | ||||
| chr19:10333302-10333323 | Rare:7 | ||||
| chr19:10333493-10333707 | Rare:74 | ||||
| chr19:10380448-10380828 | Common:12; Rare:114; Clinvar:5 | ||||
| chr19:10395020-10395342 | Rare:89 | ||||
| chr19:10653821-10654165 | Common:2; Rare:129 | ||||
| chr19:10920300-10920567 | Rare:53 | ||||
| chr19:10928388-10928850 | Common:3; Rare:132 | ||||
| chr19:11197484-11197687 | Common:1; Rare:62 | ||||
| chr19:11374877-11375239 | Common:1; Rare:115 | ||||
| chr19:11419244-11419440 | Common:1; Rare:46 | ||||
| chr19:11435109-11435440 | Common:2; Rare:86 | ||||
| chr19:11505754-11505981 | Common:1; Rare:105 |