| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50025325-50025708 | Common:7; Rare:125 | ||||
| chr19:50476216-50476547 | Common:1; Rare:156 | ||||
| chr19:50639233-50639433 | Common:1; Rare:48 | ||||
| chr19:51366335-51366551 | Common:5; Rare:57; Clinvar (benign):2 | ||||
| chr19:51927289-51927482 | Rare:62 | ||||
| chr19:52008164-52008332 | Rare:50 | ||||
| chr19:52028336-52028462 | Common:3; Rare:26 | ||||
| chr19:52171436-52171730 | Common:3; Rare:73 | ||||
| chr19:52369636-52369954 | Common:4; Rare:91 | ||||
| chr19:52397707-52397919 | Common:6; Rare:67 | ||||
| chr19:52690478-52690657 | Common:4; Rare:44 | ||||
| chr19:52735016-52735178 | Common:4; Rare:44 | ||||
| chr19:52857574-52857715 | Common:2; Rare:40 | ||||
| chr19:52897605-52897708 | Rare:33 |