Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:61901608-61901707 | Rare:24 | ||||
chr10:62049238-62049466 | Rare:53 | ||||
chr10:62268612-62268832 | Common:1; Rare:79 | ||||
chr10:63133080-63133404 | Common:2; Rare:101 | ||||
chr10:63268828-63269277 | Common:3; Rare:94 | ||||
chr10:63465958-63466051 | Rare:47 | ||||
chr10:63521751-63521998 | Common:4; Rare:87 | ||||
chr10:68075189-68075474 | Common:4; Rare:121 | ||||
chr10:68231514-68231688 | Rare:63; Clinvar (pathogenic):2 | ||||
chr10:68331871-68332145 | Common:2; Rare:113 | ||||
chr10:68332884-68332984 | Common:1; Rare:28 | ||||
chr10:68407187-68407391 | Common:4; Rare:71 | ||||
chr10:68720959-68721262 | Common:1; Rare:97 | ||||
chr10:68721469-68721548 | Rare:25 | ||||
chr10:68901049-68901368 | Common:3; Rare:126 |