| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40609899-40610168 | Common:5; Rare:53 | ||||
| chr19:40613268-40613463 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:40613537-40613606 | Rare:17 | ||||
| chr19:40613771-40614050 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:40614669-40614797 | Common:1; Rare:35 | ||||
| chr19:40690624-40691107 | Common:3; Rare:106 | ||||
| chr19:40691305-40691456 | Common:4; Rare:40 | ||||
| chr19:40715071-40715278 | Rare:55 | ||||
| chr19:40715378-40715661 | Common:2; Rare:51 | ||||
| chr19:40716239-40716303 | Rare:11 | ||||
| chr19:40716653-40717128 | Common:3; Rare:133 | ||||
| chr19:40717190-40717379 | Common:1; Rare:62 | ||||
| chr19:40749340-40749525 | Common:1; Rare:51 | ||||
| chr19:40750385-40750585 | Common:3; Rare:64 | ||||
| chr19:40750719-40750979 | Common:2; Rare:54 |