Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124418892-124419075 | Common:4; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124791816-124791956 | Rare:67 | ||||
chr10:124801751-124801835 | Rare:33 | ||||
chr10:125719462-125719734 | Common:1; Rare:86 | ||||
chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896282-125896589 | Common:2; Rare:16 | ||||
chr10:126905275-126905465 | Rare:72 | ||||
chr10:128047430-128047628 | Common:2; Rare:63 | ||||
chr10:132331817-132332209 | Common:13; Rare:126 | ||||
chr10:133308829-133309031 | Common:1; Rare:91 | ||||
chr11:207361-207719 | Common:7; Rare:110 | ||||
chr11:208688-208847 | Rare:63 | ||||
chr11:236333-236513 | Common:6; Rare:52 | ||||
chr11:236878-237052 | Common:1; Rare:65 | ||||
chr11:288817-289180 | Common:3; Rare:98 |