Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47226084-47226275 | Rare:59 | ||||
chr19:47229797-47229916 | Rare:19 | ||||
chr19:47244011-47244078 | Rare:11 | ||||
chr19:47264609-47264915 | Common:1; Rare:136 | ||||
chr19:47270266-47270570 | Common:4; Rare:97 | ||||
chr19:47277616-47277835 | Common:1; Rare:44 | ||||
chr19:47405637-47406197 | Common:1; Rare:87 | ||||
chr19:47513995-47514049 | Rare:6 | ||||
chr19:47718482-47718914 | Common:8; Rare:124 | ||||
chr19:48139688-48140090 | Common:5; Rare:84 | ||||
chr19:48328484-48328619 | Common:2; Rare:10 | ||||
chr19:48473922-48474267 | Common:3; Rare:109 | ||||
chr19:48913006-48913564 | Common:4; Rare:193 | ||||
chr19:48957691-48957955 | Common:2; Rare:50 | ||||
chr19:48969574-48969804 | Rare:69; Clinvar:1; Clinvar (benign):1 |