Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63268854-63268884 | Common:1; Rare:11 | ||||
chr10:63268900-63269388 | Common:2; Rare:92 | ||||
chr10:63465980-63466074 | Rare:45 | ||||
chr10:63521258-63521494 | Common:6; Rare:85 | ||||
chr10:63521745-63521942 | Common:4; Rare:66 | ||||
chr10:67885181-67885225 | Common:1; Rare:18 | ||||
chr10:68075162-68075466 | Common:4; Rare:124 | ||||
chr10:68231547-68231669 | Rare:36; Clinvar (pathogenic):1 | ||||
chr10:68331636-68331713 | Rare:15 | ||||
chr10:68331891-68332168 | Common:3; Rare:112 | ||||
chr10:68332887-68333037 | Common:1; Rare:38 | ||||
chr10:68407190-68407392 | Common:4; Rare:67 | ||||
chr10:68471887-68472078 | Common:1; Rare:100; Clinvar (benign):1 | ||||
chr10:68560192-68560388 | Rare:39 | ||||
chr10:68720918-68721281 | Common:3; Rare:119 |