Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113390818-113391328 | Common:3; Rare:139 | ||||
chr1:113904780-113905359 | Common:5; Rare:167; Clinvar (benign):2 | ||||
chr1:114511228-114511330 | Common:3; Rare:34 | ||||
chr1:116372989-116373539 | Common:3; Rare:180 | ||||
chr1:116374095-116374304 | Rare:61 | ||||
chr1:116387824-116388269 | Common:1; Rare:85 | ||||
chr1:116399716-116399767 | Rare:12 | ||||
chr1:116399892-116400324 | Common:3; Rare:64 | ||||
chr1:116400764-116401213 | Common:1; Rare:99; Clinvar (pathogenic):1 | ||||
chr1:116754349-116754474 | Rare:36 | ||||
chr1:117060038-117060349 | Common:7; Rare:77 | ||||
chr1:117367297-117367563 | Common:5; Rare:97 | ||||
chr1:117929547-117929821 | Common:4; Rare:84 | ||||
chr1:119140634-119140792 | Common:1; Rare:53 | ||||
chr1:119648138-119648356 | Common:3; Rare:78 |