Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151060301-151060435 | Rare:28 | ||||
chr1:151364998-151365247 | Common:1; Rare:71 | ||||
chr1:152189273-152189352 | Rare:26 | ||||
chr1:155227428-155227739 | Common:3; Rare:94 | ||||
chr1:155983382-155983518 | Rare:16 | ||||
chr1:155983571-155983780 | Rare:37 | ||||
chr1:160317262-160317294 | Rare:7 | ||||
chr1:161389941-161390210 | Common:4; Rare:52 | ||||
chr1:161530882-161531107 | Common:5; Rare:85 | ||||
chr1:170719635-170719853 | Rare:65; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:171208714-171208834 | Common:1; Rare:30 | ||||
chr1:172144405-172144498 | Rare:17 | ||||
chr1:172144541-172144892 | Rare:61 | ||||
chr1:178037910-178038133 | Rare:80 | ||||
chr1:178851284-178851338 | Rare:16 |