Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113904831-113905425 | Not yet | Common:7; Rare:176; Clinvar (benign):1 | 395 | ||
chr1:114716674-114716860 | Not yet | Common:1; Rare:77; Clinvar:4; Clinvar (benign):2 | 348 | ||
chr1:116570968-116571193 | Not yet | Common:2; Rare:66 | 177 | ||
chr1:117060159-117060359 | Not yet | Common:2; Rare:52 | 289 | ||
chr1:117929568-117929802 | Not yet | Common:3; Rare:69 | 311 | ||
chr1:119140640-119140782 | Not yet | Common:1; Rare:44 | 175 | ||
chr1:119648138-119648350 | Not yet | Common:3; Rare:77 | 218 | ||
chr1:120176310-120176621 | Not yet | Common:1; Rare:62 | 339 | ||
chr1:121184787-121185022 | Not yet | Common:1; Rare:82 | 299 | ||
chr1:145607876-145608049 | Not yet | Common:2; Rare:52 | 244 | ||
chr1:145823933-145824266 | Not yet | Rare:119 | 250 | ||
chr1:145918680-145918988 | Not yet | Common:2; Rare:65 | 379 | ||
chr1:145927364-145927644 | Not yet | Common:1; Rare:73; Clinvar (pathogenic):1 | 353 | ||
chr1:145958007-145958223 | Not yet | Rare:52 | 280 | ||
chr1:145964573-145964754 | Not yet | Rare:45 | 149 |