Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35628877-35629147 | Common:4; Rare:79 | ||||
chr19:35648110-35648393 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35740557-35740708 | Common:1; Rare:57 | ||||
chr19:35745337-35745708 | Rare:112 | ||||
chr19:35748283-35748635 | Common:3; Rare:99 | ||||
chr19:35757939-35758225 | Common:2; Rare:90 | ||||
chr19:35775246-35775635 | Common:1; Rare:100 | ||||
chr19:35782764-35783061 | Rare:70 | ||||
chr19:35784996-35785304 | Common:2; Rare:101 | ||||
chr19:35868333-35868783 | Common:1; Rare:116 | ||||
chr19:35869305-35869481 | Rare:41 | ||||
chr19:35869759-35869856 | Rare:36 | ||||
chr19:35874524-35874788 | Common:1; Rare:88 | ||||
chr19:35899680-35899884 | Common:1; Rare:59 | ||||
chr19:35900538-35900684 | Rare:33 |