Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:76047960-76048194 | Common:2; Rare:75 | ||||
chr7:76302889-76303003 | Rare:48; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr7:76303007-76303075 | Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
chr7:76625622-76625933 | Common:5; Rare:92 | ||||
chr7:77122272-77122647 | Common:2; Rare:77 | ||||
chr7:77199252-77199430 | Rare:53 | ||||
chr7:77199628-77199751 | Common:2; Rare:31 | ||||
chr7:77199775-77199906 | Rare:32 | ||||
chr7:77696236-77696481 | Rare:99 | ||||
chr7:77696757-77696960 | Rare:88 | ||||
chr7:77798355-77798951 | Common:1; Rare:144 | ||||
chr7:78627339-78627703 | Rare:68 | ||||
chr7:79453473-79453766 | Common:1; Rare:69 | ||||
chr7:79453795-79454123 | Common:2; Rare:79 | ||||
chr7:80134511-80134972 | Common:4; Rare:141 |