Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68332007-68332235 | Common:1; Rare:83 | ||||
chr10:68332860-68333032 | Common:1; Rare:45 | ||||
chr10:68333085-68333323 | Common:1; Rare:43 | ||||
chr10:68407180-68407365 | Common:4; Rare:61 | ||||
chr10:68527368-68527651 | Common:3; Rare:92 | ||||
chr10:68787952-68788264 | Common:1; Rare:78 | ||||
chr10:68956092-68956423 | Common:3; Rare:107 | ||||
chr10:68956605-68956688 | Rare:18 | ||||
chr10:68989014-68989177 | Common:1; Rare:45; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:69179940-69180354 | Common:3; Rare:144 | ||||
chr10:70146211-70146449 | Common:4; Rare:79 | ||||
chr10:70170413-70170770 | Common:4; Rare:111 | ||||
chr10:70233281-70233462 | Common:4; Rare:70; Clinvar (benign):1 | ||||
chr10:70404480-70404524 | Rare:10 | ||||
chr10:70815985-70816129 | Rare:38 |