Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:50476370-50476573 | Rare:93 | ||||
chr19:50510599-50510900 | Common:5; Rare:87 | ||||
chr19:50511152-50511276 | Rare:43 | ||||
chr19:50511337-50511610 | Common:4; Rare:84 | ||||
chr19:50639679-50639926 | Common:5; Rare:83 | ||||
chr19:50658051-50658524 | Common:1; Rare:124 | ||||
chr19:50804587-50804926 | Common:7; Rare:100 | ||||
chr19:50804957-50805130 | Common:2; Rare:48 | ||||
chr19:51108372-51108629 | Common:2; Rare:58 | ||||
chr19:51311552-51311923 | Common:4; Rare:73 | ||||
chr19:51366335-51366562 | Common:5; Rare:61; Clinvar (benign):2 | ||||
chr19:51887849-51888115 | Rare:91 | ||||
chr19:51904353-51904609 | Common:2; Rare:59 | ||||
chr19:51904923-51905146 | Common:3; Rare:70 | ||||
chr19:51927345-51927519 | Common:1; Rare:52 |