Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4061314-4061430 | Common:4; Rare:32 | ||||
chr19:4171380-4171801 | Rare:137 | ||||
chr19:4268238-4268414 | Common:4; Rare:39 | ||||
chr19:4529849-4529898 | Rare:19 | ||||
chr19:4792351-4792418 | Rare:20 | ||||
chr19:4792626-4792904 | Common:1; Rare:96 | ||||
chr19:6272221-6272314 | Rare:15 | ||||
chr19:6707075-6707541 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):4 | ||||
chr19:6717924-6717942 | Rare:4 | ||||
chr19:6718020-6718413 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
chr19:7610571-7610734 | Common:2; Rare:50 | ||||
chr19:10037439-10037611 | Common:2; Rare:38 | ||||
chr19:10070858-10071025 | Common:2; Rare:30 | ||||
chr19:10071122-10071479 | Common:2; Rare:78 | ||||
chr19:10071564-10071723 | Rare:31 |