Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:8445058-8445094 | Rare:12; Clinvar (benign):1 | ||||
chr19:9538603-9538740 | Common:1; Rare:46 | ||||
chr19:9621186-9621531 | Common:3; Rare:97 | ||||
chr19:9818806-9818859 | Rare:19 | ||||
chr19:10653835-10654019 | Common:1; Rare:66 | ||||
chr19:10928559-10928851 | Common:2; Rare:94 | ||||
chr19:11197517-11197625 | Common:1; Rare:28 | ||||
chr19:12666674-12666807 | Rare:55; Clinvar:4 | ||||
chr19:12938668-12938768 | Common:1; Rare:36 | ||||
chr19:13102534-13103003 | Common:4; Rare:109 | ||||
chr19:13116501-13116862 | Common:5; Rare:74 | ||||
chr19:13150205-13150445 | Common:1; Rare:78 | ||||
chr19:13764330-13764510 | Common:9; Rare:33 | ||||
chr19:13906080-13906328 | Rare:55 | ||||
chr19:14529261-14529635 | Common:1; Rare:151 |