Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156212878-156213029 | Common:1; Rare:39 | ||||
chr1:156282803-156282947 | Common:2; Rare:38 | ||||
chr1:156338156-156338577 | Common:2; Rare:154 | ||||
chr1:156601427-156601696 | Common:2; Rare:75 | ||||
chr1:156728402-156728476 | Common:1; Rare:14 | ||||
chr1:156751383-156751637 | Rare:67 | ||||
chr1:156767372-156767546 | Common:1; Rare:60 | ||||
chr1:158999727-159000038 | Common:2; Rare:65 | ||||
chr1:159924586-159924734 | Rare:36 | ||||
chr1:160262424-160262653 | Common:1; Rare:72 | ||||
chr1:160343173-160343389 | Rare:86 | ||||
chr1:161045888-161046042 | Common:1; Rare:39 | ||||
chr1:161118023-161118137 | Rare:54 | ||||
chr1:161132583-161132642 | Common:1; Rare:21 | ||||
chr1:161314265-161314408 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |