Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45339938-45340092 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr1:45340103-45340199 | Rare:44 | ||||
chr1:45340376-45340470 | Common:2; Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45491065-45491241 | Common:2; Rare:56 | ||||
chr1:45499998-45500043 | Common:1; Rare:7 | ||||
chr1:45500076-45500390 | Common:1; Rare:91; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521693-45522037 | Common:1; Rare:122 | ||||
chr1:45550719-45551098 | Common:3; Rare:92 | ||||
chr1:45583931-45584230 | Common:1; Rare:116 | ||||
chr1:45584456-45584819 | Common:1; Rare:123 | ||||
chr1:45686458-45686760 | Rare:114 | ||||
chr1:45687036-45687232 | Common:2; Rare:63 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45750575-45750628 | Rare:17 | ||||
chr1:45750657-45750831 | Rare:68 |