Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161225768-161226078 | Common:10; Rare:44 | ||||
chr1:161314267-161314417 | Common:3; Rare:59; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766089-161766385 | Common:3; Rare:87 | ||||
chr1:162497707-162497920 | Common:3; Rare:70 | ||||
chr1:163321752-163321997 | Common:1; Rare:64 | ||||
chr1:165768757-165769019 | Common:2; Rare:104 | ||||
chr1:166876232-166876485 | Rare:81 | ||||
chr1:167220592-167220932 | Common:1; Rare:96 | ||||
chr1:167935827-167936338 | Common:2; Rare:146 | ||||
chr1:167936561-167936757 | Common:1; Rare:64 | ||||
chr1:167936819-167937006 | Rare:77 | ||||
chr1:168225886-168226086 | Common:2; Rare:72 | ||||
chr1:169106127-169106338 | Common:2; Rare:68 | ||||
chr1:169107838-169107957 | Common:1; Rare:24 | ||||
chr1:169367784-169368250 | Common:3; Rare:87 |