Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44305001-44305145 | Rare:39 | ||||
chr19:44356645-44356818 | Common:1; Rare:31 | ||||
chr19:44448410-44448538 | Common:1; Rare:43 | ||||
chr19:44955247-44955395 | Common:2; Rare:43 | ||||
chr19:45038951-45039104 | Rare:54 | ||||
chr19:45091583-45091758 | Common:1; Rare:46 | ||||
chr19:45370552-45370803 | Common:2; Rare:73 | ||||
chr19:45507228-45507441 | Common:1; Rare:47 | ||||
chr19:45692381-45692673 | Common:1; Rare:61 | ||||
chr19:45730860-45731145 | Common:1; Rare:63 | ||||
chr19:46346941-46347124 | Common:3; Rare:56 | ||||
chr19:46471480-46471619 | Common:5; Rare:54 | ||||
chr19:46600984-46601434 | Common:5; Rare:155; Clinvar (benign):3 | ||||
chr19:47112146-47112335 | Rare:52 | ||||
chr19:47256472-47256577 | Rare:39 |