Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:132866457-132866686 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr5:132963281-132963834 | Common:4; Rare:136 | ||||
chr5:133051862-133052344 | Common:1; Rare:153 | ||||
chr5:133968525-133968707 | Rare:80 | ||||
chr5:134004648-134004869 | Common:1; Rare:82 | ||||
chr5:134004916-134005055 | Rare:30 | ||||
chr5:134226018-134226407 | Common:1; Rare:126 | ||||
chr5:134226637-134226717 | Common:1; Rare:10 | ||||
chr5:134371023-134371156 | Common:1; Rare:35 | ||||
chr5:134371395-134371612 | Common:3; Rare:97 | ||||
chr5:134411846-134412002 | Rare:51 | ||||
chr5:134632759-134632929 | Rare:34 | ||||
chr5:134648530-134648848 | Common:1; Rare:78 | ||||
chr5:134738329-134738567 | Rare:85 | ||||
chr5:134845818-134846129 | Rare:138 |