Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:47960112-47960252 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr8:47960799-47960974 | Common:1; Rare:67; Clinvar:6 | ||||
chr8:48008220-48008448 | Common:2; Rare:107 | ||||
chr8:51898955-51899331 | Common:7; Rare:165 | ||||
chr8:51899584-51899649 | Rare:12 | ||||
chr8:52714433-52714547 | Common:1; Rare:42 | ||||
chr8:54022247-54022382 | Common:1; Rare:40 | ||||
chr8:54135161-54135290 | Common:1; Rare:45 | ||||
chr8:55773306-55773512 | Common:3; Rare:73 | ||||
chr8:56074059-56074254 | Common:8; Rare:85 | ||||
chr8:56074382-56074667 | Common:4; Rare:124 | ||||
chr8:58659604-58659860 | Common:2; Rare:78 | ||||
chr8:60517124-60517208 | Rare:25 | ||||
chr8:63038766-63039002 | Common:2; Rare:81 | ||||
chr8:63168425-63168662 | Common:2; Rare:82 |