Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:73151696-73151920 | Rare:41 | ||||
chr9:74497143-74497342 | Common:3; Rare:44 | ||||
chr9:75088140-75088585 | Common:3; Rare:156 | ||||
chr9:76394376-76394572 | Common:5; Rare:83 | ||||
chr9:76459089-76459255 | Common:1; Rare:60 | ||||
chr9:78296835-78297203 | Common:2; Rare:100; Clinvar (benign):1 | ||||
chr9:81689470-81689849 | Common:10; Rare:153 | ||||
chr9:83707667-83708296 | Common:5; Rare:203 | ||||
chr9:83921428-83921634 | Common:2; Rare:80 | ||||
chr9:83979562-83979743 | Rare:61 | ||||
chr9:83980151-83980406 | Common:1; Rare:101 | ||||
chr9:83980552-83980783 | Common:3; Rare:97 | ||||
chr9:85940877-85941317 | Common:3; Rare:138 | ||||
chr9:86353999-86354617 | Rare:188 | ||||
chr9:87974521-87974648 | Common:1; Rare:27 |