Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:22822775-22822954 | Common:3; Rare:66 | ||||
chr7:23105682-23105841 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
chr7:23181840-23182077 | Common:2; Rare:96 | ||||
chr7:23531943-23532082 | Common:1; Rare:54 | ||||
chr7:24757383-24757594 | Common:3; Rare:65 | ||||
chr7:24980108-24980414 | Common:8; Rare:129 | ||||
chr7:26201417-26201815 | Common:2; Rare:187 | ||||
chr7:27095956-27096238 | Rare:77 | ||||
chr7:27113816-27113938 | Rare:27 | ||||
chr7:27150948-27151038 | Rare:22 | ||||
chr7:27152581-27152737 | Rare:28 | ||||
chr7:27179830-27179980 | Rare:58 | ||||
chr7:27185185-27185429 | Common:1; Rare:87 | ||||
chr7:27662912-27663215 | Common:7; Rare:103 | ||||
chr7:28409189-28409373 | Common:1; Rare:47 |