Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156282802-156283021 | Common:2; Rare:49 | ||||
chr1:156338169-156338539 | Common:2; Rare:135 | ||||
chr1:156728394-156728489 | Common:1; Rare:20 | ||||
chr1:156767381-156767593 | Common:1; Rare:68 | ||||
chr1:160343181-160343413 | Rare:94 | ||||
chr1:161045866-161046029 | Common:1; Rare:39 | ||||
chr1:161117955-161118146 | Rare:96 | ||||
chr1:161118230-161118370 | Rare:34 | ||||
chr1:161132426-161132667 | Common:1; Rare:88 | ||||
chr1:161196961-161197104 | Rare:20 | ||||
chr1:161197200-161197464 | Common:3; Rare:47 | ||||
chr1:161209887-161210185 | Common:1; Rare:78; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:167935974-167936261 | Common:1; Rare:87 | ||||
chr1:167936559-167936692 | Rare:44 | ||||
chr1:168225714-168226029 | Common:3; Rare:101 |