Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:42843273-42843383 | Common:2; Rare:32; Clinvar (benign):3 | ||||
chr8:42896596-42897081 | Common:1; Rare:192 | ||||
chr8:43056096-43056514 | Common:1; Rare:143 | ||||
chr8:47260781-47260991 | Common:3; Rare:93 | ||||
chr8:47960112-47960267 | Common:1; Rare:53; Clinvar (benign):1 | ||||
chr8:47960721-47960955 | Common:1; Rare:81; Clinvar:6 | ||||
chr8:48008373-48008448 | Common:1; Rare:50 | ||||
chr8:51898962-51899331 | Common:7; Rare:163 | ||||
chr8:52714184-52714571 | Common:2; Rare:142 | ||||
chr8:54022255-54022513 | Common:1; Rare:84 | ||||
chr8:55773318-55773556 | Common:3; Rare:82 | ||||
chr8:56074059-56074276 | Common:8; Rare:98 | ||||
chr8:58553075-58553297 | Rare:78 | ||||
chr8:58659311-58659472 | Common:1; Rare:59 | ||||
chr8:58659603-58659785 | Common:1; Rare:59 |