Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38336321-38336618 | Common:4; Rare:64 | ||||
chr19:38374406-38374836 | Rare:166 | ||||
chr19:38388263-38388285 | Rare:6 | ||||
chr19:38388456-38388764 | Rare:69 | ||||
chr19:38618849-38619323 | Common:4; Rare:134 | ||||
chr19:38647372-38647748 | Common:3; Rare:132 | ||||
chr19:38831756-38832076 | Common:4; Rare:97; Clinvar (benign):1 | ||||
chr19:38850391-38850720 | Common:1; Rare:113 | ||||
chr19:38852319-38852455 | Rare:40 | ||||
chr19:38899528-38900063 | Rare:161 | ||||
chr19:38930723-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39342355-39342549 | Common:2; Rare:62 | ||||
chr19:39388578-39388992 | Common:1; Rare:114 | ||||
chr19:39389191-39389495 | Common:1; Rare:79 | ||||
chr19:39390614-39390799 | Rare:41 |