Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:92253245-92253449 | Rare:47; Clinvar (pathogenic):1 | ||||
chr9:92254507-92254680 | Common:1; Rare:34 | ||||
chr9:92287879-92288276 | Rare:127 | ||||
chr9:92636103-92636197 | Rare:10 | ||||
chr9:93560388-93560528 | Common:1; Rare:15 | ||||
chr9:94122725-94123024 | Common:1; Rare:54 | ||||
chr9:94178764-94178936 | Rare:49 | ||||
chr9:94945551-94945779 | Common:1; Rare:43 | ||||
chr9:95011875-95012133 | Common:1; Rare:52 | ||||
chr9:95014714-95014980 | Rare:45 | ||||
chr9:95083285-95083863 | Common:7; Rare:198 | ||||
chr9:96419298-96419618 | Common:2; Rare:78 | ||||
chr9:96465410-96465717 | Common:1; Rare:75 | ||||
chr9:96891509-96891542 | Rare:8 | ||||
chr9:96891901-96892074 | Common:1; Rare:36 |