Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101588150-101588328 | Rare:73 | ||||
chr10:102714276-102714644 | Common:2; Rare:124 | ||||
chr10:103396432-103396727 | Rare:104 | ||||
chr10:110919326-110919647 | Common:7; Rare:88; Clinvar:1 | ||||
chr10:112446895-112447246 | Common:3; Rare:86 | ||||
chr10:118754449-118754469 | Rare:8 | ||||
chr10:119080651-119080955 | Common:4; Rare:112 | ||||
chr10:119872814-119873039 | Common:4; Rare:85 | ||||
chr10:119892627-119892777 | Common:2; Rare:61 | ||||
chr10:121928012-121928280 | Common:1; Rare:68 | ||||
chr10:122954166-122954462 | Rare:106 | ||||
chr10:123008722-123009028 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125823198-125823573 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905160-126905460 | Common:2; Rare:108 | ||||
chr10:131981894-131982139 | Common:2; Rare:89 |