Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7176327-7176445 | Common:7; Rare:52 | ||||
chr17:7203223-7203469 | Common:1; Rare:59; Clinvar (benign):1 | ||||
chr17:7215781-7215975 | Rare:20 | ||||
chr17:7311071-7311437 | Rare:93 | ||||
chr17:7330098-7330216 | Common:1; Rare:25 | ||||
chr17:7368211-7368507 | Common:3; Rare:49 | ||||
chr17:7712235-7712548 | Common:4; Rare:68 | ||||
chr17:7835500-7835921 | Common:8; Rare:127 | ||||
chr17:7836328-7836469 | Common:1; Rare:40 | ||||
chr17:7836497-7836641 | Rare:26 | ||||
chr17:7841418-7841544 | Common:1; Rare:25 | ||||
chr17:7849929-7850172 | Rare:54 | ||||
chr17:7880139-7880319 | Common:1; Rare:40 | ||||
chr17:7883822-7884172 | Common:4; Rare:50 | ||||
chr17:7885856-7886283 | Common:5; Rare:92 |