Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956185-112956440 | Common:4; Rare:117; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113929521-113929653 | Common:1; Rare:34 | ||||
chr1:114716713-114716984 | Common:4; Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
chr1:117929605-117929800 | Common:1; Rare:50 | ||||
chr1:119140634-119140771 | Common:1; Rare:43 | ||||
chr1:120176377-120176656 | Common:1; Rare:54 | ||||
chr1:145823971-145824234 | Rare:90 | ||||
chr1:145918645-145918812 | Common:1; Rare:50; Clinvar:2 | ||||
chr1:145927482-145927607 | Rare:29 | ||||
chr1:145964620-145964742 | Rare:29 | ||||
chr1:147172460-147172720 | Common:1; Rare:66 | ||||
chr1:149886680-149886918 | Rare:62 | ||||
chr1:150067618-150067833 | Common:1; Rare:58 | ||||
chr1:150629562-150629843 | Common:1; Rare:58 | ||||
chr1:150974662-150974911 | Common:2; Rare:76 |