Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36772795-36773141 | Common:4; Rare:91 | ||||
chr19:36850262-36850385 | Rare:18 | ||||
chr19:36850770-36850911 | Rare:33 | ||||
chr19:36916033-36916361 | Common:3; Rare:57 | ||||
chr19:37078328-37078476 | Common:2; Rare:36 | ||||
chr19:37218124-37218221 | Rare:21 | ||||
chr19:37317635-37317941 | Common:7; Rare:89 | ||||
chr19:37370962-37371222 | Common:3; Rare:54 | ||||
chr19:37467190-37467519 | Common:2; Rare:95 | ||||
chr19:37469173-37469357 | Common:2; Rare:51 | ||||
chr19:37506645-37506948 | Rare:65 | ||||
chr19:37594753-37594917 | Rare:46 | ||||
chr19:37779579-37779662 | Rare:18 | ||||
chr19:38618951-38619271 | Common:3; Rare:91 | ||||
chr19:38724263-38724562 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):2 |