Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155261826-155262124 | Rare:82 | ||||
chr1:155308649-155309008 | Rare:78 | ||||
chr1:155317914-155318177 | Rare:66; Clinvar (pathogenic):1 | ||||
chr1:155318473-155318830 | Common:1; Rare:74 | ||||
chr1:155320522-155320957 | Common:1; Rare:168 | ||||
chr1:155324143-155324269 | Common:1; Rare:31 | ||||
chr1:155324320-155324590 | Common:2; Rare:110 | ||||
chr1:155562724-155563028 | Common:1; Rare:158 | ||||
chr1:155563096-155563251 | Rare:65 | ||||
chr1:155859325-155859589 | Common:3; Rare:66 | ||||
chr1:155911309-155911588 | Common:2; Rare:95 | ||||
chr1:155934306-155934669 | Common:2; Rare:135 | ||||
chr1:155978150-155978244 | Rare:28 | ||||
chr1:155978430-155978937 | Common:2; Rare:137 | ||||
chr1:155979085-155979240 | Common:1; Rare:25 |