Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32486801-32487139 | Common:1; Rare:129 | ||||
chr17:32877013-32877390 | Rare:114 | ||||
chr17:34961173-34961603 | Common:3; Rare:175 | ||||
chr17:34980319-34980616 | Common:4; Rare:84 | ||||
chr17:34980652-34980917 | Common:2; Rare:82 | ||||
chr17:34981086-34981263 | Common:2; Rare:32 | ||||
chr17:35063646-35063836 | Rare:30 | ||||
chr17:35064022-35064234 | Common:1; Rare:27 | ||||
chr17:35088465-35088481 | Rare:5 | ||||
chr17:35088664-35089113 | Common:1; Rare:87 | ||||
chr17:35089174-35089628 | Common:7; Rare:104 | ||||
chr17:35119123-35119334 | Rare:61; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr17:35119551-35120016 | Common:1; Rare:159; Clinvar:18; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
chr17:35141817-35141973 | Common:1; Rare:31 | ||||
chr17:35242878-35243308 | Rare:124 |