Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:79598294-79598592 | Common:4; Rare:62 | ||||
chr17:602654-602808 | Common:1; Rare:23 | ||||
chr17:1479432-1479627 | Common:2; Rare:80 | ||||
chr17:7587248-7587541 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
chr17:16382659-16382885 | Rare:69 | ||||
chr17:16439664-16439698 | Rare:8 | ||||
chr17:30731419-30731702 | Common:3; Rare:84 | ||||
chr17:32827989-32828061 | Rare:6 | ||||
chr17:43139029-43139170 | Common:1; Rare:26 | ||||
chr17:44351424-44351671 | Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
chr17:45149404-45149614 | Common:1; Rare:77 | ||||
chr17:45149743-45150072 | Common:1; Rare:67 | ||||
chr17:45150187-45150319 | Rare:57 | ||||
chr17:45247690-45247963 | Common:1; Rare:58 | ||||
chr17:47838399-47838615 | Common:1; Rare:71 |