Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:32011010-32011190 | Common:2; Rare:59 | ||||
chr6:32011192-32011262 | Rare:20 | ||||
chr6:32011658-32011965 | Common:1; Rare:20 | ||||
chr6:32012995-32013280 | Rare:42 | ||||
chr6:32028697-32029061 | Common:1; Rare:77 | ||||
chr6:32045473-32045583 | Rare:5 | ||||
chr6:32894090-32894315 | Common:3; Rare:41 | ||||
chr6:32894689-32894838 | Common:4; Rare:48 | ||||
chr6:33425665-33425872 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
chr6:33633600-33633894 | Common:5; Rare:85 | ||||
chr6:33686937-33687065 | Rare:24 | ||||
chr6:35017335-35017637 | Common:2; Rare:83 | ||||
chr6:35242159-35242260 | Rare:31 | ||||
chr6:35720465-35720663 | Rare:30 | ||||
chr6:35731325-35731583 | Common:1; Rare:61 |