Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45011233-45011437 | Rare:52 | ||||
chr1:45011988-45012293 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45205851-45206150 | Common:1; Rare:104 | ||||
chr1:45206336-45206385 | Rare:14 | ||||
chr1:45206548-45206685 | Rare:43 | ||||
chr1:45206767-45206787 | Rare:1 | ||||
chr1:45326679-45327129 | Rare:101 | ||||
chr1:45327306-45327337 | Rare:10 | ||||
chr1:45339029-45339267 | Common:1; Rare:35 | ||||
chr1:45339807-45340379 | Common:2; Rare:205; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:45340395-45340490 | Common:1; Rare:25; Clinvar:1 | ||||
chr1:45341027-45341048 | Rare:6 | ||||
chr1:45490812-45490868 | Rare:12 | ||||
chr1:45491053-45491450 | Common:3; Rare:104 | ||||
chr1:45499894-45500385 | Common:2; Rare:119; Clinvar:5; Clinvar (pathogenic):3 |