| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5580144-5580308 | Common:1; Rare:24 | ||||
| chr19:5585443-5585758 | Common:2; Rare:65 | ||||
| chr19:5686485-5686691 | Rare:47 | ||||
| chr19:5691385-5691557 | Common:1; Rare:73 | ||||
| chr19:5695480-5695804 | Common:6; Rare:103 | ||||
| chr19:5718625-5718971 | Common:1; Rare:59 | ||||
| chr19:5773045-5773254 | Common:3; Rare:42 | ||||
| chr19:5773751-5773999 | Common:1; Rare:37 | ||||
| chr19:5802279-5802466 | Rare:42 | ||||
| chr19:5803978-5804367 | Common:1; Rare:69 | ||||
| chr19:5804923-5805091 | Common:2; Rare:66 | ||||
| chr19:5826681-5826809 | Rare:20 | ||||
| chr19:5827859-5828471 | Common:7; Rare:215; Clinvar (benign):1 | ||||
| chr19:5828856-5828988 | Common:5; Rare:23 | ||||
| chr19:5889749-5889909 | Rare:35 |