Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:36828741-36829283 | Common:3; Rare:215 | ||||
chr18:46098231-46098595 | Common:11; Rare:104; Clinvar (benign):6 | ||||
chr18:46104225-46104394 | Common:2; Rare:44 | ||||
chr18:46917452-46917609 | Rare:68 | ||||
chr18:46946611-46946836 | Common:2; Rare:51 | ||||
chr18:47930820-47930974 | Rare:55 | ||||
chr18:49460586-49460798 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr18:49813645-49814211 | Common:2; Rare:199 | ||||
chr18:50878963-50879127 | Common:3; Rare:52 | ||||
chr18:55321725-55321925 | Rare:44 | ||||
chr18:55322331-55322482 | Rare:31 | ||||
chr18:55510667-55510807 | Rare:24 | ||||
chr18:55510930-55511128 | Rare:43 | ||||
chr18:56651129-56651418 | Common:4; Rare:76 | ||||
chr18:58671232-58671430 | Rare:89 |