Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124092373-124092511 | Rare:37 | ||||
chr10:124418892-124419060 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124791798-124791942 | Common:1; Rare:73 | ||||
chr10:124801771-124801841 | Rare:25 | ||||
chr10:125719480-125719739 | Common:1; Rare:88 | ||||
chr10:125823179-125823594 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 | ||||
chr10:125896474-125896589 | Rare:4 | ||||
chr10:126905061-126905493 | Common:3; Rare:153 | ||||
chr10:128047430-128047635 | Common:2; Rare:66 | ||||
chr10:130136321-130136504 | Common:7; Rare:71 | ||||
chr10:132331803-132332216 | Common:16; Rare:137 | ||||
chr10:133308835-133309013 | Common:1; Rare:86 | ||||
chr11:207343-207719 | Common:8; Rare:128 | ||||
chr11:208688-208860 | Rare:70 | ||||
chr11:236316-236483 | Common:6; Rare:55 |