Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:23680813-23680956 | Common:2; Rare:33 | ||||
chr7:24979252-24979558 | Common:7; Rare:81 | ||||
chr7:24979581-24979668 | Common:2; Rare:54 | ||||
chr7:26101576-26101689 | Common:2; Rare:16 | ||||
chr7:26193252-26193696 | Rare:156; Clinvar (benign):2 | ||||
chr7:28955569-28955912 | Rare:124 | ||||
chr7:28956075-28956210 | Common:1; Rare:45 | ||||
chr7:28956591-28956796 | Common:1; Rare:76 | ||||
chr7:29684610-29684646 | Rare:5 | ||||
chr7:29684887-29685022 | Common:1; Rare:50 | ||||
chr7:29685608-29685644 | Common:3; Rare:10 | ||||
chr7:32727970-32728146 | Common:1; Rare:58 | ||||
chr7:32728568-32728823 | Common:9; Rare:81 | ||||
chr7:32942454-32942659 | Common:1; Rare:55 | ||||
chr7:36970456-36970779 | Common:3; Rare:57 |