Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:51074024-51074334 | Common:5; Rare:77 | ||||
chr10:51074364-51074575 | Common:1; Rare:48; Clinvar (benign):2 | ||||
chr10:56361232-56361518 | Common:6; Rare:103 | ||||
chr10:58268964-58269295 | Common:4; Rare:112 | ||||
chr10:58385343-58385599 | Common:2; Rare:81 | ||||
chr10:59176369-59176698 | Common:6; Rare:109 | ||||
chr10:59177035-59177161 | Rare:31 | ||||
chr10:60572523-60572644 | Rare:26 | ||||
chr10:60733389-60733583 | Rare:53 | ||||
chr10:62268595-62268912 | Common:1; Rare:116 | ||||
chr10:63465958-63466168 | Common:3; Rare:103 | ||||
chr10:63521190-63521489 | Common:7; Rare:106 | ||||
chr10:63521789-63521949 | Common:4; Rare:61 | ||||
chr10:66925746-66926070 | Common:2; Rare:67 | ||||
chr10:68075189-68075484 | Common:4; Rare:125 |