Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:7183158-7183261 | Common:1; Rare:38 | ||||
chr7:15688144-15688428 | Common:2; Rare:83 | ||||
chr7:16644767-16644875 | Rare:35 | ||||
chr7:16989939-16990267 | Common:2; Rare:66 | ||||
chr7:20329518-20329766 | Rare:39 | ||||
chr7:22563167-22563373 | Common:1; Rare:48 | ||||
chr7:22727744-22727806 | Rare:18 | ||||
chr7:22855022-22855139 | Common:1; Rare:32 | ||||
chr7:23013028-23013248 | Common:1; Rare:41 | ||||
chr7:23490426-23490556 | Common:3; Rare:54 | ||||
chr7:26195604-26195852 | Common:2; Rare:116; Clinvar (benign):1 | ||||
chr7:27096936-27097133 | Common:1; Rare:54 | ||||
chr7:27098038-27098071 | Rare:6 | ||||
chr7:27118087-27118207 | Common:1; Rare:24 | ||||
chr7:29684876-29685017 | Rare:50 |