Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:112183706-112183818 | Common:2; Rare:40 | ||||
chr10:112446892-112447430 | Common:3; Rare:148 | ||||
chr10:112950127-112950313 | Common:3; Rare:37 | ||||
chr10:113854182-113854885 | Common:1; Rare:155 | ||||
chr10:114821667-114821996 | Rare:104 | ||||
chr10:117005062-117005355 | Common:2; Rare:92 | ||||
chr10:117374739-117375084 | Common:1; Rare:130 | ||||
chr10:117542201-117542408 | Rare:52 | ||||
chr10:117542556-117542763 | Common:1; Rare:49 | ||||
chr10:118046723-118047008 | Common:4; Rare:93 | ||||
chr10:118754906-118755288 | Common:1; Rare:129 | ||||
chr10:119080772-119080927 | Rare:62 | ||||
chr10:119165650-119165802 | Rare:68; Clinvar (benign):3 | ||||
chr10:119178786-119178876 | Common:2; Rare:38 | ||||
chr10:119596458-119596543 | Rare:33 |