Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15976072-15976213 | Common:2; Rare:35 | ||||
chr1:16352420-16352606 | Common:3; Rare:99 | ||||
chr1:16366982-16367264 | Common:1; Rare:84 | ||||
chr1:16440550-16440759 | Common:1; Rare:56 | ||||
chr1:16613525-16613665 | |||||
chr1:16921767-16921932 | Rare:25 | ||||
chr1:17053994-17054320 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):8 | ||||
chr1:17439669-17439887 | Rare:71 | ||||
chr1:19210254-19210515 | Rare:88 | ||||
chr1:19251512-19251857 | Common:6; Rare:114 | ||||
chr1:19485460-19485765 | Rare:116 | ||||
chr1:19596869-19597064 | Common:2; Rare:91 | ||||
chr1:20661326-20661730 | Common:3; Rare:148; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786564-20786859 | Rare:107 | ||||
chr1:20787244-20787437 | Rare:93 |