Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119080698-119080999 | Common:3; Rare:121 | ||||
chr10:119596475-119596729 | Common:1; Rare:75 | ||||
chr10:119892527-119892769 | Common:3; Rare:92 | ||||
chr10:120851207-120851411 | Common:4; Rare:71 | ||||
chr10:122954188-122954458 | Rare:98 | ||||
chr10:123008773-123009023 | Common:6; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125719456-125719709 | Rare:77 | ||||
chr10:125823193-125823563 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905277-126905461 | Rare:70 | ||||
chr10:131981916-131982138 | Common:1; Rare:83 | ||||
chr10:132307896-132308149 | Common:4; Rare:76 | ||||
chr10:132331821-132332120 | Common:11; Rare:93 | ||||
chr10:133308829-133308980 | Rare:71 | ||||
chr11:207335-207720 | Common:8; Rare:130 | ||||
chr11:208610-208854 | Rare:86 |