Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63521789-63521984 | Common:4; Rare:76 | ||||
chr10:68231540-68231625 | Rare:25; Clinvar (pathogenic):1 | ||||
chr10:68331886-68332157 | Common:2; Rare:113 | ||||
chr10:68332877-68332966 | Common:1; Rare:25 | ||||
chr10:68407185-68407458 | Common:5; Rare:91 | ||||
chr10:68720977-68721259 | Common:1; Rare:92 | ||||
chr10:68900988-68901361 | Common:3; Rare:148 | ||||
chr10:68956100-68956203 | Rare:45 | ||||
chr10:68988657-68988856 | Common:1; Rare:63; Clinvar (benign):2 | ||||
chr10:69087967-69088203 | Rare:53 | ||||
chr10:71773494-71773795 | Common:4; Rare:87 | ||||
chr10:72216255-72216547 | Common:3; Rare:85 | ||||
chr10:72273662-72273938 | Rare:70 | ||||
chr10:72354893-72355023 | Common:2; Rare:68 | ||||
chr10:72626026-72626361 | Common:2; Rare:81 |