Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:42541700-42541897 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr8:42843277-42843508 | Common:2; Rare:67; Clinvar (benign):3 | ||||
chr8:42896676-42897031 | Common:1; Rare:147 | ||||
chr8:47260787-47260981 | Common:3; Rare:84 | ||||
chr8:47960094-47960273 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr8:47960811-47960974 | Common:1; Rare:65; Clinvar:6 | ||||
chr8:48008345-48008460 | Common:2; Rare:71 | ||||
chr8:51898988-51899281 | Common:5; Rare:139 | ||||
chr8:52714427-52714557 | Common:1; Rare:53 | ||||
chr8:53843230-53843358 | Rare:28 | ||||
chr8:54135173-54135290 | Common:1; Rare:42 | ||||
chr8:55773371-55773498 | Common:3; Rare:44 | ||||
chr8:56074445-56074669 | Common:3; Rare:99 | ||||
chr8:58659652-58659992 | Common:3; Rare:91 | ||||
chr8:61714492-61714752 | Common:1; Rare:76 |