Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780539-114780748 | Rare:82 | ||||
chr1:115768667-115768965 | Common:6; Rare:64; Clinvar:7; Clinvar (benign):2 | ||||
chr1:117929599-117929792 | Rare:54 | ||||
chr1:119140628-119140735 | Rare:32 | ||||
chr1:120176358-120176647 | Common:1; Rare:57 | ||||
chr1:145823917-145824251 | Rare:117 | ||||
chr1:145918693-145919005 | Common:2; Rare:62 | ||||
chr1:145927425-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964607-145964742 | Rare:32 | ||||
chr1:146228953-146229187 | Common:2; Rare:53 | ||||
chr1:147172420-147172783 | Common:1; Rare:94 | ||||
chr1:148679744-148679909 | Rare:17 | ||||
chr1:149812217-149812547 | Common:2; Rare:147 | ||||
chr1:149850902-149851064 | |||||
chr1:149886630-149887004 | Common:2; Rare:141 |