Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619699-112619842 | Common:1; Rare:52 | ||||
chr1:112707071-112707267 | Rare:69 | ||||
chr1:112956025-112956353 | Common:4; Rare:112; Clinvar:12; Clinvar (benign):3 | ||||
chr1:113073095-113073225 | Common:1; Rare:45 | ||||
chr1:113905010-113905365 | Common:3; Rare:102 | ||||
chr1:114716665-114716985 | Common:4; Rare:122; Clinvar:5; Clinvar (benign):3 | ||||
chr1:117367297-117367502 | Common:4; Rare:76 | ||||
chr1:117929618-117929841 | Common:3; Rare:60 | ||||
chr1:119140627-119140771 | Common:1; Rare:46 | ||||
chr1:145823930-145824219 | Rare:101 | ||||
chr1:145918658-145919002 | Common:2; Rare:82; Clinvar:1 | ||||
chr1:145927480-145927612 | Rare:31 | ||||
chr1:145964595-145964742 | Rare:33 | ||||
chr1:145996503-145996767 | Rare:105 | ||||
chr1:147172450-147172782 | Common:1; Rare:83 |