Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39996958-39997063 | Common:4; Rare:31 | ||||
chr19:40056167-40056269 | Rare:16 | ||||
chr19:40348512-40348727 | Common:3; Rare:67 | ||||
chr19:40715056-40715145 | Rare:29 | ||||
chr19:40798867-40799265 | Common:6; Rare:144 | ||||
chr19:41310385-41310484 | Rare:18 | ||||
chr19:41397324-41397576 | Common:4; Rare:63 | ||||
chr19:41883150-41883243 | Rare:20 | ||||
chr19:41956843-41957069 | Rare:73 | ||||
chr19:42075837-42076209 | Rare:103 | ||||
chr19:42268232-42268554 | Rare:64 | ||||
chr19:42302351-42302505 | Rare:41 | ||||
chr19:43527147-43527335 | Common:5; Rare:71; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43580444-43580654 | Common:4; Rare:36 | ||||
chr19:43595980-43596327 | Common:5; Rare:106 |