Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:120851167-120851433 | Common:5; Rare:92 | ||||
chr10:121927961-121928094 | Common:1; Rare:43 | ||||
chr10:121928427-121928522 | Rare:29 | ||||
chr10:122954186-122954506 | Common:1; Rare:118 | ||||
chr10:122980316-122980473 | Common:1; Rare:36 | ||||
chr10:123008791-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092369-124092568 | Common:1; Rare:51 | ||||
chr10:124791785-124791938 | Common:1; Rare:80 | ||||
chr10:124801735-124801830 | Rare:33 | ||||
chr10:125719456-125719739 | Common:1; Rare:94 | ||||
chr10:125823207-125823567 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905271-126905460 | Rare:72 | ||||
chr10:130136321-130136469 | Common:6; Rare:60 | ||||
chr10:132331818-132332229 | Common:13; Rare:131 | ||||
chr10:133308835-133308982 | Rare:69 |