Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:6757865-6758103 | Common:5; Rare:92 | ||||
chr9:8858195-8858220 | Rare:6 | ||||
chr9:14313545-14313736 | Common:1; Rare:48 | ||||
chr9:15422591-15422880 | Common:1; Rare:122 | ||||
chr9:15552794-15552992 | Common:1; Rare:81 | ||||
chr9:18473944-18474206 | Rare:70 | ||||
chr9:19102877-19103053 | Common:2; Rare:73 | ||||
chr9:19127450-19127722 | Common:5; Rare:85 | ||||
chr9:19380165-19380339 | Common:5; Rare:90 | ||||
chr9:26892731-26892895 | Common:1; Rare:79 | ||||
chr9:26947146-26947242 | Rare:32 | ||||
chr9:26956255-26956460 | Common:2; Rare:77 | ||||
chr9:27573430-27573570 | Common:5; Rare:81 | ||||
chr9:32384449-32384724 | Common:1; Rare:97 | ||||
chr9:33001565-33001911 | Common:3; Rare:129; Clinvar (benign):3 |