| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10655789-10656083 | Common:1; Rare:82 | ||||
| chr19:10671191-10671442 | Common:1; Rare:67 | ||||
| chr19:10683510-10683788 | Common:3; Rare:111 | ||||
| chr19:10836268-10836551 | Common:2; Rare:72 | ||||
| chr19:10928563-10928865 | Common:2; Rare:99 | ||||
| chr19:11089377-11089528 | Rare:32; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr19:11197487-11197679 | Common:1; Rare:60 | ||||
| chr19:11374882-11375241 | Common:1; Rare:114 | ||||
| chr19:11381175-11381463 | Common:2; Rare:95; Clinvar:1 | ||||
| chr19:11435075-11435440 | Common:2; Rare:95 | ||||
| chr19:11435598-11435758 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11435924-11436197 | Rare:89; Clinvar:1 | ||||
| chr19:11505776-11506069 | Common:2; Rare:112 | ||||
| chr19:11529069-11529294 | Rare:43 | ||||
| chr19:11559195-11559465 | Common:4; Rare:82 |