Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007682-110008017 | Rare:102 | ||||
chr10:110919134-110919340 | Common:1; Rare:51 | ||||
chr10:110919348-110919616 | Common:7; Rare:69 | ||||
chr10:112183743-112183821 | Common:2; Rare:30 | ||||
chr10:112446899-112447274 | Common:3; Rare:90 | ||||
chr10:113854369-113854634 | Rare:53 | ||||
chr10:117005269-117005366 | Common:2; Rare:26 | ||||
chr10:118754921-118755295 | Common:1; Rare:120 | ||||
chr10:119080780-119080929 | Rare:61 | ||||
chr10:119165661-119165755 | Rare:45; Clinvar (benign):3 | ||||
chr10:119818416-119818749 | Rare:105 | ||||
chr10:119892558-119892777 | Common:3; Rare:82 | ||||
chr10:120851187-120851438 | Common:5; Rare:90 | ||||
chr10:122954202-122954484 | Rare:104 | ||||
chr10:123008806-123009006 | Common:5; Rare:58; Clinvar:3; Clinvar (benign):5 |