Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75784595-75784896 | Common:2; Rare:132 | ||||
chr17:75878540-75878727 | Common:3; Rare:68 | ||||
chr17:75979081-75979274 | Rare:53; Clinvar:4 | ||||
chr17:75979381-75979587 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr17:76103712-76103867 | Common:4; Rare:49 | ||||
chr17:76353612-76353676 | Rare:27 | ||||
chr17:76384380-76384659 | Common:3; Rare:73 | ||||
chr17:76481629-76481670 | Rare:4 | ||||
chr17:76537586-76537780 | Common:1; Rare:55 | ||||
chr17:76537904-76538212 | Common:1; Rare:96 | ||||
chr17:76585771-76586035 | Common:5; Rare:71 | ||||
chr17:76726471-76726872 | Common:5; Rare:147 | ||||
chr17:76737309-76737465 | Common:3; Rare:66 | ||||
chr17:76737901-76738001 | Common:1; Rare:33 | ||||
chr17:77140654-77141080 | Common:2; Rare:146 |