Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16644644-16644773 | Common:1; Rare:2 | ||||
chr1:16913896-16914121 | Common:8; Rare:48 | ||||
chr1:16978852-16978994 | Common:2; Rare:35 | ||||
chr1:20644241-20644540 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:20654360-20654629 | Common:3; Rare:78; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:20656124-20656276 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr1:21855521-21855913 | Common:4; Rare:132; Clinvar:9; Clinvar (benign):5 | ||||
chr1:21857147-21857372 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr1:21907947-21908057 | Rare:13 | ||||
chr1:22025185-22025544 | Common:7; Rare:95 | ||||
chr1:22509954-22510157 | Common:1; Rare:33 | ||||
chr1:24151290-24151505 | Common:1; Rare:42 | ||||
chr1:25875508-25875765 | Rare:69 | ||||
chr1:27428768-27429134 | Common:2; Rare:77 | ||||
chr1:27525603-27525746 | Common:1; Rare:25 |