| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49929451-49929820 | Common:7; Rare:128 | ||||
| chr19:50476242-50476547 | Rare:144 | ||||
| chr19:50511185-50511269 | Rare:30 | ||||
| chr19:51026588-51026754 | Common:2; Rare:43 | ||||
| chr19:51366335-51366562 | Common:5; Rare:61; Clinvar (benign):2 | ||||
| chr19:51751852-51752014 | Common:2; Rare:37 | ||||
| chr19:52008164-52008339 | Rare:50 | ||||
| chr19:52397715-52397885 | Common:3; Rare:52 | ||||
| chr19:52690478-52690673 | Common:4; Rare:50 | ||||
| chr19:52786735-52786880 | Common:8; Rare:41 | ||||
| chr19:52897605-52897808 | Rare:60 | ||||
| chr19:52962851-52963026 | Common:3; Rare:58 | ||||
| chr19:53193333-53193490 | Common:1; Rare:32 | ||||
| chr19:53254814-53255042 | Common:2; Rare:80 | ||||
| chr19:53333742-53333768 | Rare:13 |