Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:128520555-128520787 | Common:1; Rare:86 | ||||
chr6:128883463-128883598 | Common:2; Rare:30 | ||||
chr6:130366167-130366478 | Common:3; Rare:66 | ||||
chr6:131628120-131628433 | Common:3; Rare:85 | ||||
chr6:131950900-131951217 | Rare:90 | ||||
chr6:132814304-132814611 | Common:3; Rare:116 | ||||
chr6:133953064-133953269 | Common:2; Rare:71 | ||||
chr6:134174848-134175061 | Common:1; Rare:103 | ||||
chr6:135054784-135054950 | Common:6; Rare:51 | ||||
chr6:135497604-135497834 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289761-136290032 | Common:1; Rare:117 | ||||
chr6:137219111-137219199 | Common:1; Rare:23 | ||||
chr6:137219256-137219487 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr6:137866944-137867233 | Rare:65 | ||||
chr6:138404167-138404569 | Common:7; Rare:111 |