Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780547-114780735 | Rare:75 | ||||
chr1:115089462-115089612 | Common:2; Rare:56 | ||||
chr1:117060077-117060341 | Common:6; Rare:61 | ||||
chr1:117929546-117929792 | Common:1; Rare:74 | ||||
chr1:119140628-119140767 | Rare:45 | ||||
chr1:120176385-120176598 | Rare:49 | ||||
chr1:121184756-121185077 | Common:1; Rare:108 | ||||
chr1:145823885-145824257 | Rare:133 | ||||
chr1:145918693-145919013 | Common:2; Rare:65 | ||||
chr1:145927415-145927618 | Common:1; Rare:56; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964754 | Rare:45 | ||||
chr1:145996531-145996813 | Rare:112 | ||||
chr1:147172429-147172779 | Common:1; Rare:90 | ||||
chr1:149812349-149812611 | Common:1; Rare:76 | ||||
chr1:149850848-149851062 | Rare:1 |