Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15684518-15684611 | Rare:22; Clinvar:1 | ||||
chr1:15756133-15756351 | Common:2; Rare:26 | ||||
chr1:15764363-15764695 | Common:3; Rare:64 | ||||
chr1:15776892-15777258 | Rare:91 | ||||
chr1:15847503-15847887 | Rare:135 | ||||
chr1:15976042-15976185 | Common:2; Rare:36 | ||||
chr1:16155946-16156184 | Rare:55; Clinvar:2 | ||||
chr1:16237152-16237307 | Rare:50 | ||||
chr1:16352417-16352768 | Common:4; Rare:143 | ||||
chr1:16980582-16980958 | Common:5; Rare:105 | ||||
chr1:16981006-16981216 | Rare:35 | ||||
chr1:17011866-17012060 | Common:1; Rare:55; Clinvar:2 | ||||
chr1:17053947-17054331 | Common:3; Rare:121; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17439293-17439492 | Common:1; Rare:31 | ||||
chr1:17439500-17439535 | Rare:6 |