| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51311552-51311899 | Common:4; Rare:69 | ||||
| chr19:51366335-51366585 | Common:8; Rare:69; Clinvar (benign):2 | ||||
| chr19:51751852-51751994 | Common:2; Rare:28 | ||||
| chr19:51887861-51888095 | Rare:77 | ||||
| chr19:51904928-51905146 | Common:3; Rare:70 | ||||
| chr19:51927320-51927517 | Common:1; Rare:62 | ||||
| chr19:51986782-51987002 | Common:1; Rare:59 | ||||
| chr19:52008130-52008359 | Rare:69 | ||||
| chr19:52028313-52028475 | Common:3; Rare:40 | ||||
| chr19:52048626-52048908 | Common:2; Rare:83 | ||||
| chr19:52139873-52140155 | Common:2; Rare:77 | ||||
| chr19:52171419-52171768 | Common:3; Rare:89 | ||||
| chr19:52269431-52269603 | Common:1; Rare:60 | ||||
| chr19:52296996-52297208 | Common:18; Rare:51 | ||||
| chr19:52336128-52336347 | Common:5; Rare:76 |