Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45406363-45406649 | Common:1; Rare:62 | ||||
chr19:45423477-45423797 | Common:3; Rare:66; Clinvar (benign):1 | ||||
chr19:45730889-45731100 | Common:1; Rare:46 | ||||
chr19:46601000-46601370 | Common:4; Rare:123 | ||||
chr19:47256460-47256568 | Rare:39 | ||||
chr19:48170285-48170669 | Common:2; Rare:106 | ||||
chr19:48325424-48325594 | Common:2; Rare:42 | ||||
chr19:48619139-48619516 | Common:1; Rare:125 | ||||
chr19:49157789-49157835 | Rare:14 | ||||
chr19:49487387-49487644 | Common:4; Rare:96 | ||||
chr19:49580543-49580686 | Rare:45 | ||||
chr19:49929430-49929539 | Common:2; Rare:37 | ||||
chr19:51366339-51366608 | Common:8; Rare:74; Clinvar (benign):2 | ||||
chr19:52397727-52397879 | Common:3; Rare:47 | ||||
chr19:54115638-54115787 | Common:1; Rare:31; Clinvar:4 |