Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91500728-91500890 | Common:2; Rare:52 | ||||
chr1:91886048-91886352 | Rare:125 | ||||
chr1:92298945-92299074 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92784615-92784883 | Common:2; Rare:75 | ||||
chr1:92831874-92832113 | Common:1; Rare:107; Clinvar:6; Clinvar (benign):5 | ||||
chr1:93079097-93079280 | Common:2; Rare:81 | ||||
chr1:93179612-93179922 | Common:2; Rare:51 | ||||
chr1:93180064-93180280 | Rare:78 | ||||
chr1:93180291-93180721 | Common:1; Rare:172 | ||||
chr1:93345777-93346152 | Common:5; Rare:133 | ||||
chr1:93448002-93448158 | Common:2; Rare:57 | ||||
chr1:93879125-93879308 | Common:3; Rare:68 | ||||
chr1:94237530-94237728 | Rare:81 | ||||
chr1:94418254-94418464 | Common:2; Rare:75 | ||||
chr1:94541751-94541991 | Rare:70 |