Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:123008722-123009044 | Common:6; Rare:92; Clinvar:4; Clinvar (benign):5 | ||||
chr10:123154355-123154901 | Common:3; Rare:160 | ||||
chr10:124461730-124461860 | Common:4; Rare:49 | ||||
chr10:124791776-124791936 | Common:1; Rare:86 | ||||
chr10:124801694-124801901 | Rare:69 | ||||
chr10:125719438-125719721 | Rare:89 | ||||
chr10:125823030-125823717 | Common:3; Rare:233; Clinvar:2; Clinvar (benign):3 | ||||
chr10:125896239-125896621 | Common:5; Rare:30 | ||||
chr10:126905290-126905468 | Rare:67 | ||||
chr10:131939839-131940172 | Common:4; Rare:76 | ||||
chr10:131981759-131982154 | Common:4; Rare:137 | ||||
chr10:132331843-132332116 | Common:10; Rare:76 | ||||
chr10:133308829-133308968 | Rare:66 | ||||
chr10:133309873-133310287 | Rare:131 | ||||
chr11:207314-207780 | Common:9; Rare:150 |