| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476209-50476542 | Common:1; Rare:156 | ||||
| chr19:51366333-51366544 | Common:5; Rare:55; Clinvar (benign):2 | ||||
| chr19:51927362-51927487 | Common:1; Rare:36 | ||||
| chr19:51986826-51987003 | Common:1; Rare:43 | ||||
| chr19:52008166-52008290 | Rare:38 | ||||
| chr19:52028360-52028462 | Common:2; Rare:18 | ||||
| chr19:52189660-52190088 | Common:4; Rare:156 | ||||
| chr19:52269431-52269603 | Common:1; Rare:60 | ||||
| chr19:52397733-52397907 | Common:4; Rare:57 | ||||
| chr19:52638332-52638489 | Common:3; Rare:47 | ||||
| chr19:52690475-52690638 | Common:4; Rare:36 | ||||
| chr19:52897596-52897819 | Rare:67 | ||||
| chr19:52962861-52963090 | Common:3; Rare:71 | ||||
| chr19:53254808-53255019 | Common:1; Rare:71 | ||||
| chr19:53333563-53333775 | Common:4; Rare:68 |