Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150076986-150077386 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150149600-150150360 | Common:20; Rare:863 | ||||
chr1:150150384-150151519 | Common:10; Rare:365 | ||||
chr1:150233852-150235040 | Common:12; Rare:493 | ||||
chr1:150235552-150236409 | Common:12; Rare:682 | ||||
chr1:150236435-150236835 | Common:5; Rare:87 | ||||
chr1:150257600-150257960 | Common:1; Rare:81 | ||||
chr1:150267928-150268501 | Common:3; Rare:298 | ||||
chr1:150268456-150269332 | Common:2; Rare:551 | ||||
chr1:150293692-150293979 | Common:5; Rare:313 | ||||
chr1:150293917-150294317 | Common:5; Rare:97 | ||||
chr1:150321328-150321623 | Rare:329; Clinvar:15; Clinvar (benign):5 | ||||
chr1:150321551-150321951 | Rare:76 | ||||
chr1:150363420-150363790 | Common:3; Rare:207 | ||||
chr1:150363790-150364315 | Common:29; Rare:659 |