Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7395014-7395189 | Common:6; Rare:53 | ||||
chr19:7489017-7489053 | Rare:16 | ||||
chr19:7629529-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636997-7637143 | Common:2; Rare:49; Clinvar (benign):1 | ||||
chr19:7943649-7943990 | Rare:87 | ||||
chr19:8321322-8321703 | Common:2; Rare:153 | ||||
chr19:8363850-8364162 | Common:3; Rare:68 | ||||
chr19:8390077-8390453 | Common:2; Rare:109 | ||||
chr19:8832207-8832318 | Rare:38 | ||||
chr19:9435501-9435640 | Common:1; Rare:56 | ||||
chr19:9538603-9538736 | Common:1; Rare:45 | ||||
chr19:9621192-9621529 | Common:3; Rare:94 | ||||
chr19:9675029-9675149 | Rare:32 | ||||
chr19:9793147-9793492 | Rare:71 | ||||
chr19:9818809-9818868 | Rare:25 |