Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66654240-66654567 | Common:2; Rare:109 | ||||
chr7:66844878-66845065 | Common:2; Rare:78 | ||||
chr7:67302409-67302692 | Common:5; Rare:92 | ||||
chr7:73005893-73006096 | Rare:17 | ||||
chr7:74890549-74890812 | Common:2; Rare:77 | ||||
chr7:81690403-81690528 | Rare:28 | ||||
chr7:94409318-94409608 | Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:100335891-100336138 | Common:1; Rare:77 | ||||
chr7:131108088-131108196 | Rare:15 | ||||
chr8:6532398-6532709 | Common:4; Rare:91 | ||||
chr8:6661456-6661775 | Common:1; Rare:85 | ||||
chr8:98030266-98030483 | Rare:40 | ||||
chr8:98367339-98367405 | Common:1; Rare:13 | ||||
chr9:66269907-66270047 | Common:1; Rare:27 | ||||
chr9:70413083-70413115 | Rare:6 |