Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122375210-122375430 | Common:2; Rare:59 | ||||
chr10:122879531-122879691 | Common:3; Rare:44 | ||||
chr10:122954186-122954464 | Rare:102 | ||||
chr10:123008781-123009028 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124093497-124093618 | Common:1; Rare:24 | ||||
chr10:124461696-124461863 | Common:5; Rare:58 | ||||
chr10:124791775-124791942 | Common:1; Rare:87 | ||||
chr10:125719466-125719739 | Common:1; Rare:92 | ||||
chr10:125823200-125823604 | Common:1; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896443-125896628 | Common:5; Rare:19 | ||||
chr10:126905312-126905475 | Rare:61 | ||||
chr10:128047485-128047645 | Common:3; Rare:47 | ||||
chr10:129466930-129467296 | Common:5; Rare:156; Clinvar:1 | ||||
chr10:132331847-132332216 | Common:12; Rare:107 | ||||
chr10:133308063-133308319 | Common:1; Rare:57 |