Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:57989636-57989665 | Rare:4 | ||||
chr17:57990881-57991060 | Common:1; Rare:32 | ||||
chr17:57991637-57991930 | Common:3; Rare:46 | ||||
chr17:57992516-57992771 | Common:3; Rare:49 | ||||
chr17:57995283-57995333 | Rare:8 | ||||
chr17:57997401-57997562 | Rare:35 | ||||
chr17:58324369-58324510 | Rare:36 | ||||
chr17:58659248-58659556 | Common:5; Rare:134 | ||||
chr17:59001610-59001941 | Rare:78; Clinvar:2 | ||||
chr17:59681028-59681731 | Common:2; Rare:146; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:59682359-59682790 | Rare:77 | ||||
chr17:59786493-59786781 | Rare:53 | ||||
chr17:59829405-59829595 | Common:1; Rare:23 | ||||
chr17:59839144-59839311 | Rare:40 | ||||
chr17:59839573-59839835 | Rare:46 |