Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:23490417-23490574 | Common:3; Rare:67 | ||||
chr7:26193345-26193694 | Rare:127; Clinvar (benign):2 | ||||
chr7:26449842-26449994 | Rare:21 | ||||
chr7:32728737-32728869 | Common:7; Rare:48 | ||||
chr7:38358258-38358480 | Common:5; Rare:92 | ||||
chr7:44019117-44019389 | Common:2; Rare:97 | ||||
chr7:44467664-44467882 | Common:3; Rare:40 | ||||
chr7:44986599-44986756 | Common:2; Rare:80 | ||||
chr7:45768930-45769121 | Common:1; Rare:57 | ||||
chr7:65750908-65751099 | Common:2; Rare:82 | ||||
chr7:66493543-66493762 | Common:3; Rare:92 | ||||
chr7:66654452-66654567 | Rare:42 | ||||
chr7:67302402-67302696 | Common:5; Rare:95 | ||||
chr7:73005886-73006154 | Rare:22 | ||||
chr7:74890532-74890836 | Common:2; Rare:102 |