Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209431506-209431564 | Rare:10 | ||||
chr1:209431922-209431944 | Rare:5 | ||||
chr1:209431993-209432214 | Rare:71 | ||||
chr1:209432337-209432392 | Common:1; Rare:14 | ||||
chr1:209433273-209433951 | Common:5; Rare:135 | ||||
chr1:209434362-209434412 | Common:1; Rare:8 | ||||
chr1:209435280-209435381 | Common:1; Rare:17 | ||||
chr1:209542674-209542883 | Common:2; Rare:33 | ||||
chr1:209567767-209567863 | Common:2; Rare:16 | ||||
chr1:209609635-209609869 | Common:1; Rare:63 | ||||
chr1:209611508-209611767 | Common:2; Rare:65 | ||||
chr1:209623886-209623921 | Common:1; Rare:14; Clinvar (benign):1 | ||||
chr1:209649397-209649587 | Common:1; Rare:31 | ||||
chr1:209655880-209656188 | Common:1; Rare:49 | ||||
chr1:209657176-209657535 | Common:2; Rare:63 |