Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:166973018-166973064 | Rare:6 | ||||
chr1:174445955-174446163 | Common:1; Rare:44 | ||||
chr1:175008361-175008680 | Common:2; Rare:72 | ||||
chr1:177170730-177170993 | Common:1; Rare:58 | ||||
chr1:178371313-178371401 | Common:7; Rare:33 | ||||
chr1:178372028-178372118 | Rare:19 | ||||
chr1:178542645-178542790 | Common:5; Rare:50 | ||||
chr1:180502281-180502298 | Rare:10 | ||||
chr1:183261033-183261261 | Rare:53; Clinvar (pathogenic):1 | ||||
chr1:183471159-183471436 | Common:2; Rare:49 | ||||
chr1:185316209-185316366 | Rare:34 | ||||
chr1:197201221-197201548 | Common:1; Rare:110 | ||||
chr1:197910400-197910631 | Common:1; Rare:57 | ||||
chr1:197910914-197911157 | Common:13; Rare:67 | ||||
chr1:198291158-198291265 | Rare:16 |