Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36687366-36687624 | Common:2; Rare:82 | ||||
chr19:36838350-36838453 | Common:1; Rare:32 | ||||
chr19:36850775-36850915 | Rare:35 | ||||
chr19:36916013-36916358 | Common:3; Rare:57 | ||||
chr19:37078143-37078483 | Common:4; Rare:79 | ||||
chr19:37218144-37218260 | Rare:16 | ||||
chr19:37317666-37317911 | Common:6; Rare:59 | ||||
chr19:37467177-37467516 | Common:2; Rare:99 | ||||
chr19:37469280-37469405 | Common:1; Rare:38 | ||||
chr19:37551268-37551389 | Rare:43 | ||||
chr19:37594753-37594886 | Rare:37 | ||||
chr19:37779579-37779653 | Rare:18 | ||||
chr19:37907014-37907284 | Common:1; Rare:62 | ||||
chr19:38647372-38647763 | Common:3; Rare:133 | ||||
chr19:38831765-38832052 | Common:4; Rare:83; Clinvar (benign):1 |