Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49896878-49897014 | Common:1; Rare:18 | ||||
chr19:49929451-49929773 | Common:7; Rare:109 | ||||
chr19:50025335-50025748 | Common:7; Rare:130 | ||||
chr19:50476209-50476547 | Common:1; Rare:160 | ||||
chr19:50511169-50511299 | Rare:44 | ||||
chr19:50983906-50984168 | Common:1; Rare:73 | ||||
chr19:51001142-51001271 | Common:2; Rare:33 | ||||
chr19:51017284-51017310 | Rare:13 | ||||
chr19:51019397-51019495 | Rare:28 | ||||
chr19:51019675-51019989 | Common:5; Rare:57 | ||||
chr19:51026547-51026754 | Common:2; Rare:56 | ||||
chr19:51027558-51027622 | Rare:14 | ||||
chr19:51027666-51027887 | Common:1; Rare:34 | ||||
chr19:51366294-51366551 | Common:5; Rare:79; Clinvar (benign):2 | ||||
chr19:51723953-51724155 | Rare:51 |