Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54715550-54715940 | Common:5; Rare:117 | ||||
chr1:54764424-54764893 | Common:7; Rare:138; Clinvar (benign):1 | ||||
chr1:54887165-54887454 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr1:55039255-55039597 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
chr1:55214457-55214737 | Common:3; Rare:78 | ||||
chr1:55215329-55215560 | Rare:85 | ||||
chr1:56579357-56579504 | Rare:41 | ||||
chr1:56645108-56645424 | Common:1; Rare:103 | ||||
chr1:58546010-58546440 | Common:4; Rare:89 | ||||
chr1:58546735-58547004 | Common:2; Rare:93 | ||||
chr1:58700005-58700239 | Common:4; Rare:102 | ||||
chr1:58783999-58784410 | Common:1; Rare:105 | ||||
chr1:59296478-59296834 | Common:12; Rare:90 | ||||
chr1:59296870-59297170 | Common:3; Rare:85 | ||||
chr1:59392900-59393360 | Common:5; Rare:127 |