Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:151330177-151330595 | Common:3; Rare:72 | ||||
chr6:151330628-151330659 | Rare:3 | ||||
chr6:152151347-152151590 | Common:3; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
chr6:152253763-152253812 | Rare:10 | ||||
chr6:152992909-152993038 | Rare:35 | ||||
chr6:153000613-153000899 | Common:4; Rare:37 | ||||
chr6:154410634-154410996 | Common:6; Rare:66 | ||||
chr6:154791910-154791993 | Common:2; Rare:18 | ||||
chr6:156782003-156782025 | Rare:1 | ||||
chr6:156946413-156946712 | Common:3; Rare:57 | ||||
chr6:157020936-157021042 | Common:1; Rare:27 | ||||
chr6:157056147-157056195 | Common:1; Rare:11 | ||||
chr6:157824088-157824431 | Common:2; Rare:60 | ||||
chr6:157909663-157909987 | Common:1; Rare:64 | ||||
chr6:157938688-157938800 | Common:3; Rare:33 |