Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:23490413-23490568 | Common:3; Rare:64 | ||||
chr7:25387354-25387402 | Rare:9 | ||||
chr7:25662853-25663007 | Common:1; Rare:28 | ||||
chr7:25855129-25855351 | Rare:49 | ||||
chr7:25856936-25857242 | Common:11; Rare:83 | ||||
chr7:26193249-26193695 | Rare:156; Clinvar (benign):2 | ||||
chr7:26376052-26376268 | Common:2; Rare:66 | ||||
chr7:26440302-26440365 | Rare:11 | ||||
chr7:26658254-26658357 | Rare:16 | ||||
chr7:28956652-28956780 | Rare:48 | ||||
chr7:29988597-29988677 | Rare:33 | ||||
chr7:32728719-32728949 | Common:8; Rare:72 | ||||
chr7:33803168-33803260 | Rare:25 | ||||
chr7:35036606-35036887 | Common:1; Rare:55 | ||||
chr7:35186106-35186475 | Common:1; Rare:101 |