Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76727127-76727322 | Common:2; Rare:62 | ||||
chr17:76736416-76736716 | Common:1; Rare:163 | ||||
chr17:76737056-76737764 | Common:7; Rare:275 | ||||
chr17:76737815-76738151 | Common:4; Rare:98 | ||||
chr17:77088497-77088892 | Common:3; Rare:103 | ||||
chr17:77127927-77127988 | Rare:10 | ||||
chr17:77140248-77141061 | Common:5; Rare:258 | ||||
chr17:77141584-77141735 | Common:1; Rare:29 | ||||
chr17:77144350-77144652 | Common:1; Rare:57 | ||||
chr17:77281126-77281508 | Common:6; Rare:158 | ||||
chr17:77281631-77281687 | Rare:10 | ||||
chr17:77319372-77319693 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
chr17:77319913-77319993 | Common:1; Rare:25; Clinvar:2; Clinvar (benign):1 | ||||
chr17:77322470-77322689 | Common:1; Rare:42 | ||||
chr17:77322770-77322869 | Common:1; Rare:24 |