Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:123008782-123009023 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124418875-124419092 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
chr10:124449996-124450179 | Rare:47 | ||||
chr10:124461715-124461873 | Common:4; Rare:58 | ||||
chr10:124791742-124791959 | Common:1; Rare:113 | ||||
chr10:124801706-124801830 | Rare:43 | ||||
chr10:125719453-125719802 | Common:1; Rare:132 | ||||
chr10:125823200-125823566 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896282-125896589 | Common:2; Rare:16 | ||||
chr10:126905297-126905464 | Rare:64 | ||||
chr10:129466930-129467240 | Common:4; Rare:133 | ||||
chr10:131981853-131982154 | Common:4; Rare:111 | ||||
chr10:133237691-133237883 | Rare:52 | ||||
chr10:133308835-133308974 | Rare:66 | ||||
chr10:133357678-133357788 | Common:1; Rare:18 |