Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37467177-37467529 | Common:2; Rare:101 | ||||
chr19:37551270-37551395 | Rare:42 | ||||
chr19:37779579-37779662 | Rare:18 | ||||
chr19:37907140-37907300 | Rare:30 | ||||
chr19:38256336-38256493 | Common:2; Rare:36 | ||||
chr19:38374413-38374812 | Rare:148 | ||||
chr19:38618832-38619307 | Common:4; Rare:135 | ||||
chr19:38647372-38647769 | Common:3; Rare:133 | ||||
chr19:38647833-38647905 | Rare:5 | ||||
chr19:38899528-38900034 | Rare:155 | ||||
chr19:38930722-38931002 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39342356-39342488 | Common:2; Rare:38 | ||||
chr19:39391025-39391425 | Common:1; Rare:161 | ||||
chr19:39406684-39406880 | Rare:72 | ||||
chr19:39435854-39436163 | Common:6; Rare:112 |