| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50804978-50805092 | Common:1; Rare:32 | ||||
| chr19:51366271-51366619 | Common:8; Rare:107; Clinvar (benign):2 | ||||
| chr19:51751818-51751983 | Common:2; Rare:33 | ||||
| chr19:51887869-51888048 | Rare:64 | ||||
| chr19:52008164-52008339 | Rare:50 | ||||
| chr19:52028336-52028475 | Common:3; Rare:29 | ||||
| chr19:52028568-52028869 | Rare:60 | ||||
| chr19:52048641-52048685 | Rare:8 | ||||
| chr19:52296996-52297200 | Common:18; Rare:48 | ||||
| chr19:52369851-52369973 | Common:1; Rare:47 | ||||
| chr19:52397711-52397880 | Common:3; Rare:50 | ||||
| chr19:52638334-52638540 | Common:4; Rare:53 | ||||
| chr19:52735021-52735167 | Common:3; Rare:39 | ||||
| chr19:52786704-52786871 | Common:9; Rare:48 | ||||
| chr19:52897599-52897762 | Rare:48 |