| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11447200-11447630 | Common:6; Rare:143; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:11505010-11505666 | Common:5; Rare:512 | ||||
| chr19:11505686-11505979 | Common:2; Rare:244 | ||||
| chr19:11529004-11529349 | Common:2; Rare:165 | ||||
| chr19:11559114-11559514 | Common:11; Rare:277 | ||||
| chr19:11597254-11597626 | Common:6; Rare:257 | ||||
| chr19:11597560-11597810 | Common:4; Rare:126 | ||||
| chr19:11738792-11739338 | Common:12; Rare:363 | ||||
| chr19:11766889-11767128 | Rare:62 | ||||
| chr19:11798396-11798702 | Common:2; Rare:65 | ||||
| chr19:11814039-11814437 | Common:4; Rare:208 | ||||
| chr19:11887636-11887886 | Common:1; Rare:74 | ||||
| chr19:11888042-11888222 | Common:2; Rare:39 | ||||
| chr19:11924909-11925287 | Common:18; Rare:276 | ||||
| chr19:11964837-11965121 | Common:1; Rare:62 |