Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:67696087-67696305 | Rare:42 | ||||
chr10:67885085-67885203 | Rare:46 | ||||
chr10:68075050-68075131 | Common:1; Rare:15 | ||||
chr10:68075161-68075466 | Common:4; Rare:124 | ||||
chr10:68331910-68332134 | Common:1; Rare:97 | ||||
chr10:68332884-68332962 | Common:1; Rare:22 | ||||
chr10:68407185-68407375 | Common:4; Rare:67 | ||||
chr10:68527422-68527733 | Common:3; Rare:104 | ||||
chr10:68721140-68721555 | Common:4; Rare:128 | ||||
chr10:68901039-68901368 | Common:3; Rare:127 | ||||
chr10:68956091-68956231 | Rare:62 | ||||
chr10:68988598-68988856 | Common:1; Rare:72; Clinvar (benign):2 | ||||
chr10:69179943-69180353 | Common:3; Rare:141 | ||||
chr10:69318570-69318965 | Common:5; Rare:109 | ||||
chr10:69451210-69451628 | Common:2; Rare:110 |