Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38930742-38931013 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390969-39391431 | Common:1; Rare:176 | ||||
chr19:39406552-39406931 | Common:1; Rare:112 | ||||
chr19:39407031-39407106 | Rare:14 | ||||
chr19:39846313-39846473 | Common:1; Rare:75 | ||||
chr19:39970917-39971223 | Common:4; Rare:88 | ||||
chr19:39996955-39997074 | Common:4; Rare:37 | ||||
chr19:40056163-40056260 | Rare:15 | ||||
chr19:40090864-40090978 | Common:1; Rare:35 | ||||
chr19:40266088-40266267 | Rare:32 | ||||
chr19:40285186-40285623 | Common:3; Rare:144 | ||||
chr19:40341876-40341975 | Rare:25 | ||||
chr19:40348337-40348739 | Common:4; Rare:129 | ||||
chr19:40465611-40466096 | Common:3; Rare:165 | ||||
chr19:40716880-40717015 | Common:1; Rare:46 |