Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156767372-156767546 | Common:1; Rare:60 | ||||
chr1:157138342-157138607 | Common:3; Rare:79 | ||||
chr1:159925461-159925617 | Common:1; Rare:42 | ||||
chr1:160205269-160205459 | Common:2; Rare:54 | ||||
chr1:160343181-160343396 | Rare:90 | ||||
chr1:161045888-161046042 | Common:1; Rare:39 | ||||
chr1:161118000-161118141 | Rare:73 | ||||
chr1:161132426-161132703 | Common:1; Rare:95 | ||||
chr1:161159404-161159517 | Common:1; Rare:31 | ||||
chr1:161314267-161314414 | Common:3; Rare:56; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749719-161749851 | Rare:48 | ||||
chr1:161750228-161750427 | Rare:49 | ||||
chr1:161766133-161766363 | Common:3; Rare:67 | ||||
chr1:163321733-163322075 | Common:1; Rare:92 | ||||
chr1:165768757-165769052 | Common:2; Rare:119 |