Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140634-119140768 | Common:1; Rare:42 | ||||
chr1:120176343-120176614 | Common:1; Rare:57 | ||||
chr1:145823917-145824249 | Rare:117 | ||||
chr1:145859070-145859179 | Rare:26 | ||||
chr1:145918671-145919002 | Common:2; Rare:75; Clinvar:1 | ||||
chr1:145927422-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964749 | Rare:44 | ||||
chr1:146228950-146229167 | Common:3; Rare:53 | ||||
chr1:147928280-147928441 | Common:1; Rare:51 | ||||
chr1:149850793-149851064 | Rare:8 | ||||
chr1:149886642-149887031 | Common:3; Rare:145 | ||||
chr1:149887908-149888215 | Rare:93 | ||||
chr1:149936840-149936940 | Rare:19 | ||||
chr1:150067689-150067884 | Rare:58 | ||||
chr1:150235963-150236163 | Common:1; Rare:49 |