Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113904831-113905425 | Common:7; Rare:176; Clinvar (benign):1 | ||||
chr1:114716674-114716860 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):2 | ||||
chr1:116570968-116571193 | Common:2; Rare:66 | ||||
chr1:117060159-117060359 | Common:2; Rare:52 | ||||
chr1:117929568-117929802 | Common:3; Rare:69 | ||||
chr1:119140640-119140782 | Common:1; Rare:44 | ||||
chr1:119648138-119648350 | Common:3; Rare:77 | ||||
chr1:120176310-120176621 | Common:1; Rare:62 | ||||
chr1:121184787-121185022 | Common:1; Rare:82 | ||||
chr1:145607876-145608049 | Common:2; Rare:52 | ||||
chr1:145823933-145824266 | Rare:119 | ||||
chr1:145918680-145918988 | Common:2; Rare:65 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 | ||||
chr1:145964573-145964754 | Rare:45 |