Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38899552-38900041 | Rare:151 | ||||
chr19:38930742-38930987 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39335987-39336186 | Rare:55 | ||||
chr19:39390860-39391425 | Common:1; Rare:212 | ||||
chr19:39406699-39407038 | Rare:125 | ||||
chr19:39407362-39408103 | Common:2; Rare:202 | ||||
chr19:39413681-39413812 | Rare:22 | ||||
chr19:39414201-39414269 | Rare:15 | ||||
chr19:39970958-39971223 | Common:3; Rare:73 | ||||
chr19:39996956-39997101 | Common:4; Rare:50 | ||||
chr19:40056163-40056253 | Rare:15 | ||||
chr19:40090873-40091006 | Common:1; Rare:34 | ||||
chr19:40348388-40348724 | Common:4; Rare:110 | ||||
chr19:40408156-40408377 | Rare:42; Clinvar:5 | ||||
chr19:40413336-40413548 | Rare:60 |