Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32342080-32342235 | Rare:45 | ||||
chr17:32350012-32350323 | Rare:136 | ||||
chr17:34156732-34157073 | Rare:67 | ||||
chr17:34157673-34157947 | Common:4; Rare:51 | ||||
chr17:34961440-34961579 | Common:1; Rare:65 | ||||
chr17:34962304-34962673 | Rare:88 | ||||
chr17:34980378-34980607 | Common:4; Rare:66 | ||||
chr17:35119795-35120145 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr17:35242900-35243081 | Rare:60 | ||||
chr17:35432422-35432749 | Common:2; Rare:55 | ||||
chr17:35448716-35448977 | Common:2; Rare:50 | ||||
chr17:35578531-35578661 | Common:1; Rare:30; Clinvar (benign):1 | ||||
chr17:35587135-35587641 | Common:1; Rare:129 | ||||
chr17:35809295-35809576 | Rare:119 | ||||
chr17:35930720-35930897 | Rare:62 |