Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155911230-155911800 | Common:5; Rare:267; Clinvar (benign):1 | ||||
chr1:155934269-155934663 | Common:3; Rare:243 | ||||
chr1:155941397-155941638 | Rare:74 | ||||
chr1:155978128-155978292 | Common:2; Rare:72 | ||||
chr1:155978451-155978684 | Common:2; Rare:129 | ||||
chr1:155979073-155979274 | Common:2; Rare:67 | ||||
chr1:156002494-156002965 | Common:2; Rare:75 | ||||
chr1:156020811-156021061 | Rare:133 | ||||
chr1:156053755-156053931 | Rare:89 | ||||
chr1:156054560-156054950 | Common:7; Rare:179 | ||||
chr1:156082240-156082750 | Common:1; Rare:145 | ||||
chr1:156106320-156106728 | Common:4; Rare:130 | ||||
chr1:156114491-156114900 | Common:2; Rare:163; Clinvar:8; Clinvar (benign):7 | ||||
chr1:156126164-156126555 | Rare:147; Clinvar:1; Clinvar (benign):1 | ||||
chr1:156193724-156194203 | Common:6; Rare:187 |