Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86704532-86704932 | Common:3; Rare:149 | ||||
chr1:86914323-86914632 | Common:1; Rare:78 | ||||
chr1:87329082-87329159 | Common:1; Rare:16 | ||||
chr1:88684064-88684355 | Common:3; Rare:79 | ||||
chr1:88992600-88992972 | Common:3; Rare:96 | ||||
chr1:89065188-89065440 | Common:1; Rare:38 | ||||
chr1:89994981-89995170 | Common:2; Rare:75 | ||||
chr1:92298945-92299079 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93180360-93180721 | Common:1; Rare:160 | ||||
chr1:93345772-93345925 | Common:4; Rare:60 | ||||
chr1:93448018-93448158 | Common:1; Rare:54 | ||||
chr1:93879144-93879270 | Common:1; Rare:42 | ||||
chr1:94541730-94541991 | Rare:76 | ||||
chr1:94927042-94927446 | Common:1; Rare:135 | ||||
chr1:95233955-95234248 | Common:5; Rare:93 |