Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149240376-149240770 | Rare:6 | ||||
chr1:154947427-154947673 | Common:2; Rare:68 | ||||
chr1:156130385-156130633 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160135144-160135511 | Common:1; Rare:93; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
chr1:167455013-167455076 | Rare:14 | ||||
chr1:174160118-174160435 | Common:1; Rare:68 | ||||
chr1:178098281-178098581 | Common:1; Rare:45 | ||||
chr1:179970122-179970184 | Rare:14 | ||||
chr1:197201250-197201511 | Common:1; Rare:87 | ||||
chr1:201359622-201359736 | Common:1; Rare:31; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:201362386-201362401 | Rare:7; Clinvar:1; Clinvar (benign):1 | ||||
chr1:202495273-202495682 | Common:1; Rare:110 | ||||
chr1:203629982-203630056 | Rare:9 | ||||
chr1:204410894-204411187 | Common:1; Rare:122 | ||||
chr1:206659255-206659369 | Common:1; Rare:14 |