Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155308576-155309045 | Common:2; Rare:186 | ||||
chr1:155323810-155323964 | Rare:35 | ||||
chr1:155324142-155324569 | Common:5; Rare:252 | ||||
chr1:155562359-155562994 | Common:3; Rare:509 | ||||
chr1:155563088-155563284 | Rare:129 | ||||
chr1:155609970-155610300 | Common:5; Rare:117; Clinvar (pathogenic):1 | ||||
chr1:155688640-155689134 | Common:3; Rare:213 | ||||
chr1:155857166-155857366 | Rare:99 | ||||
chr1:155859315-155859502 | Common:2; Rare:71 | ||||
chr1:155934335-155934572 | Common:2; Rare:174 | ||||
chr1:155941398-155941598 | Rare:62 | ||||
chr1:155978478-155978613 | Rare:33 | ||||
chr1:155978525-155978669 | Common:1; Rare:44 | ||||
chr1:155979060-155979400 | Common:4; Rare:104 | ||||
chr1:156020838-156021069 | Rare:135 |