Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113905002-113905381 | Common:4; Rare:112 | ||||
chr1:114152914-114153067 | Common:3; Rare:44 | ||||
chr1:114153810-114154050 | Rare:61 | ||||
chr1:114581542-114581841 | Common:1; Rare:131 | ||||
chr1:114757933-114758103 | Common:3; Rare:55 | ||||
chr1:114780547-114780745 | Rare:78 | ||||
chr1:117060072-117060332 | Common:5; Rare:56 | ||||
chr1:117605794-117606048 | Rare:72 | ||||
chr1:117929591-117929795 | Rare:56 | ||||
chr1:119140629-119140724 | Rare:30 | ||||
chr1:120176446-120176598 | Rare:39 | ||||
chr1:145823936-145824260 | Rare:115 | ||||
chr1:145918693-145918779 | Common:1; Rare:22 | ||||
chr1:145927394-145927644 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964742 | Rare:45 |