Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:116960151-116960422 | Rare:63 | ||||
chr10:117005122-117005254 | Rare:46 | ||||
chr10:118754924-118755348 | Common:2; Rare:138 | ||||
chr10:119080630-119080734 | Common:3; Rare:27 | ||||
chr10:119080755-119080955 | Rare:83 | ||||
chr10:119178783-119178969 | Common:3; Rare:69 | ||||
chr10:119596960-119597199 | Common:1; Rare:66 | ||||
chr10:119892500-119892769 | Common:3; Rare:98 | ||||
chr10:120851200-120851472 | Common:6; Rare:101 | ||||
chr10:121928003-121928047 | Rare:14 | ||||
chr10:121928438-121928466 | Rare:7 | ||||
chr10:122879570-122879816 | Common:4; Rare:57 | ||||
chr10:122954188-122954474 | Rare:105 | ||||
chr10:123008727-123009039 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125823143-125823577 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 |