Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:47260781-47260981 | Common:3; Rare:87 | ||||
chr8:47960084-47960242 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr8:47960683-47961012 | Common:2; Rare:126; Clinvar:10; Clinvar (benign):1 | ||||
chr8:51898984-51899255 | Common:5; Rare:128 | ||||
chr8:52714418-52714540 | Common:1; Rare:49 | ||||
chr8:53843212-53843353 | Rare:33 | ||||
chr8:54022255-54022514 | Common:1; Rare:85 | ||||
chr8:54135132-54135322 | Common:3; Rare:59 | ||||
chr8:55773288-55773531 | Common:3; Rare:86 | ||||
chr8:56074374-56074602 | Common:4; Rare:109 | ||||
chr8:58553126-58553287 | Rare:56 | ||||
chr8:58659652-58659905 | Common:2; Rare:68 | ||||
chr8:61714106-61714275 | Common:1; Rare:41 | ||||
chr8:61714315-61714752 | Common:3; Rare:138 | ||||
chr8:63038739-63038950 | Common:3; Rare:79 |