Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:33731920-33731970 | Rare:10 | ||||
chr18:34331518-34331650 | Common:1; Rare:46 | ||||
chr18:48937492-48937721 | Rare:60 | ||||
chr18:48951855-48952178 | Common:4; Rare:73 | ||||
chr18:49021504-49021755 | Common:1; Rare:54 | ||||
chr18:49953315-49953624 | Common:3; Rare:63 | ||||
chr18:54426223-54426524 | Rare:52 | ||||
chr18:57658838-57658970 | Common:1; Rare:15 | ||||
chr18:57662485-57662823 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr18:57679968-57679994 | Rare:4 | ||||
chr18:57701041-57701144 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
chr18:57710592-57710668 | Rare:12 | ||||
chr18:57719497-57719599 | Common:2; Rare:34 | ||||
chr18:57784954-57784977 | Rare:4 | ||||
chr18:57802008-57802288 | Common:2; Rare:73 |