Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15457014-15457174 | Common:2; Rare:49 | ||||
chr1:15526600-15526905 | Common:2; Rare:97 | ||||
chr1:15946200-15946448 | Common:1; Rare:60 | ||||
chr1:16018035-16018266 | Common:5; Rare:78 | ||||
chr1:16352420-16352530 | Common:1; Rare:58 | ||||
chr1:16948675-16948755 | Rare:18 | ||||
chr1:19210247-19210538 | Common:1; Rare:94 | ||||
chr1:19251512-19251838 | Common:6; Rare:106 | ||||
chr1:19288539-19288877 | Common:7; Rare:131 | ||||
chr1:19312006-19312333 | Common:8; Rare:157 | ||||
chr1:19485435-19485737 | Common:1; Rare:101 | ||||
chr1:19799866-19800196 | Common:5; Rare:92 | ||||
chr1:19815092-19815441 | Common:5; Rare:70 | ||||
chr1:20661349-20661705 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21345463-21345655 | Common:2; Rare:75 |