Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:52314254-52314300 | Rare:13 | ||||
chr10:56361236-56361459 | Common:5; Rare:70 | ||||
chr10:58385322-58385516 | Common:1; Rare:69 | ||||
chr10:60778260-60778533 | Common:1; Rare:64 | ||||
chr10:62049209-62049482 | Common:1; Rare:61 | ||||
chr10:62816349-62816527 | Rare:29 | ||||
chr10:63465963-63466090 | Rare:57 | ||||
chr10:68075183-68075466 | Common:4; Rare:120 | ||||
chr10:68331914-68332134 | Common:1; Rare:96 | ||||
chr10:68332877-68332962 | Common:1; Rare:25 | ||||
chr10:68407196-68407440 | Common:5; Rare:80 | ||||
chr10:68471887-68472028 | Common:1; Rare:76; Clinvar (benign):1 | ||||
chr10:68721091-68721262 | Common:1; Rare:53 | ||||
chr10:68901049-68901368 | Common:3; Rare:126 | ||||
chr10:68956093-68956242 | Rare:65 |