Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86704718-86704902 | Common:2; Rare:70 | ||||
chr1:88683962-88684350 | Common:3; Rare:115 | ||||
chr1:89994981-89995174 | Common:2; Rare:75 | ||||
chr1:91021998-91022341 | Rare:90 | ||||
chr1:91500751-91500909 | Common:2; Rare:52 | ||||
chr1:92298945-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079037-93079280 | Common:3; Rare:110 | ||||
chr1:93179626-93179954 | Common:1; Rare:60 | ||||
chr1:93180302-93180758 | Common:2; Rare:184 | ||||
chr1:93345820-93345925 | Common:2; Rare:38 | ||||
chr1:93879144-93879273 | Common:1; Rare:43 | ||||
chr1:94418217-94418464 | Common:2; Rare:84 | ||||
chr1:94541751-94541991 | Rare:70 | ||||
chr1:94927048-94927456 | Common:1; Rare:135 | ||||
chr1:95233955-95234233 | Common:5; Rare:83 |