Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117060210-117060359 | Common:2; Rare:46 | ||||
chr1:117929591-117929787 | Rare:54 | ||||
chr1:119140604-119140683 | Rare:41; Clinvar (pathogenic):1 | ||||
chr1:119648138-119648364 | Common:3; Rare:79 | ||||
chr1:120069578-120069925 | Common:7; Rare:72 | ||||
chr1:120176306-120176647 | Common:1; Rare:63 | ||||
chr1:145823922-145824286 | Rare:128 | ||||
chr1:145918689-145919022 | Common:2; Rare:74 | ||||
chr1:145927370-145927644 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr1:145957983-145958270 | Rare:64 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:145994916-145995449 | Rare:224 | ||||
chr1:145996015-145996210 | Rare:82 | ||||
chr1:145996513-145996829 | Rare:123 | ||||
chr1:146228980-146229167 | Common:2; Rare:40 |