Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113812239-113812579 | Common:2; Rare:138 | ||||
chr1:113905022-113905416 | Common:5; Rare:111 | ||||
chr1:114581587-114581792 | Rare:93 | ||||
chr1:114716656-114716885 | Common:1; Rare:95; Clinvar:5; Clinvar (benign):3 | ||||
chr1:114757947-114758112 | Common:3; Rare:49 | ||||
chr1:115089462-115089612 | Common:2; Rare:56 | ||||
chr1:117929568-117929800 | Common:2; Rare:69 | ||||
chr1:119140634-119140764 | Rare:41 | ||||
chr1:120176328-120176596 | Rare:56 | ||||
chr1:145823922-145824251 | Rare:115 | ||||
chr1:145858996-145859161 | Rare:47 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927385-145927597 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964747 | Rare:44 | ||||
chr1:147172427-147172779 | Common:1; Rare:91 |