Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58150766-58150898 | Common:4; Rare:41 | ||||
chr19:58183275-58183445 | Rare:58 | ||||
chr19:58228721-58228964 | Common:2; Rare:88 | ||||
chr19:58278611-58278987 | Common:3; Rare:114 | ||||
chr19:58305152-58305442 | Common:3; Rare:97 | ||||
chr19:58326880-58327000 | Common:1; Rare:27 | ||||
chr19:58346917-58347162 | Common:1; Rare:77 | ||||
chr19:58347602-58347779 | Common:8; Rare:85 | ||||
chr19:58386725-58386807 | Common:1; Rare:22 | ||||
chr19:58408445-58408752 | Common:4; Rare:94 | ||||
chr19:58499216-58499550 | Common:2; Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
chr19:58519743-58520017 | Rare:69 | ||||
chr19:58538751-58538931 | Rare:69 | ||||
chr19:58544159-58544480 | Common:4; Rare:139 | ||||
chr19:58554997-58555248 | Common:2; Rare:86 |