| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10380454-10380824 | Common:12; Rare:109; Clinvar:5 | ||||
| chr19:10503271-10503421 | Rare:32 | ||||
| chr19:10568974-10569223 | Common:2; Rare:64 | ||||
| chr19:10653817-10653897 | Rare:30 | ||||
| chr19:10928537-10928692 | Common:1; Rare:40 | ||||
| chr19:10960689-10961087 | Common:3; Rare:158 | ||||
| chr19:11018683-11019042 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):5 | ||||
| chr19:11033907-11034198 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):7 | ||||
| chr19:11089336-11089539 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11090356-11090610 | Common:2; Rare:79 | ||||
| chr19:11197504-11197637 | Common:1; Rare:40 | ||||
| chr19:11203408-11203657 | Rare:61 | ||||
| chr19:11419274-11419408 | Common:1; Rare:31 | ||||
| chr19:11435335-11435709 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:11559195-11559397 | Common:1; Rare:61 |