Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:59964661-59964908 | Common:2; Rare:100 | ||||
chr17:60078591-60078698 | Rare:35 | ||||
chr17:60078840-60079101 | Common:6; Rare:98 | ||||
chr17:60305206-60305411 | Rare:47 | ||||
chr17:60392025-60392646 | Common:4; Rare:178 | ||||
chr17:60421362-60421503 | Common:1; Rare:30 | ||||
chr17:60421637-60421754 | Rare:30 | ||||
chr17:60525799-60526031 | Common:2; Rare:77 | ||||
chr17:60526060-60526449 | Common:1; Rare:126 | ||||
chr17:60599731-60599838 | Rare:25 | ||||
chr17:60599869-60600389 | Common:4; Rare:179 | ||||
chr17:60600764-60601021 | Rare:46; Clinvar (benign):1 | ||||
chr17:60677276-60677444 | Common:1; Rare:36 | ||||
chr17:60677694-60677931 | Common:1; Rare:64 | ||||
chr17:61863027-61863212 | Rare:44 |