| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46601176-46601425 | Common:4; Rare:74; Clinvar (benign):2 | ||||
| chr19:46608286-46608577 | Common:1; Rare:67; Clinvar (benign):6 | ||||
| chr19:46717080-46717237 | Common:2; Rare:51 | ||||
| chr19:46745841-46746061 | Common:3; Rare:45 | ||||
| chr19:46850231-46850384 | Rare:21 | ||||
| chr19:47256440-47256577 | Rare:49 | ||||
| chr19:47349073-47349397 | Rare:92 | ||||
| chr19:47745343-47745562 | Rare:92 | ||||
| chr19:47780664-47780746 | Common:1; Rare:27 | ||||
| chr19:48170270-48170706 | Common:2; Rare:117 | ||||
| chr19:48390469-48390561 | Rare:24 | ||||
| chr19:48391439-48391590 | Rare:45 | ||||
| chr19:48445888-48446191 | Common:1; Rare:120 | ||||
| chr19:48619139-48619441 | Common:1; Rare:96 | ||||
| chr19:48619480-48619606 | Rare:43 |