Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100535841-100535952 | Common:6; Rare:52 | ||||
chr10:100912751-100913024 | Common:1; Rare:84 | ||||
chr10:100913335-100913355 | Rare:7 | ||||
chr10:100987445-100987598 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101588166-101588329 | Rare:69 | ||||
chr10:101694865-101695211 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr10:101783367-101783479 | Rare:51 | ||||
chr10:101818425-101818778 | Common:1; Rare:85 | ||||
chr10:102056100-102056348 | Common:1; Rare:57 | ||||
chr10:102132879-102133071 | Rare:45 | ||||
chr10:102152083-102152413 | Common:3; Rare:107 | ||||
chr10:102245209-102245555 | Common:1; Rare:56 | ||||
chr10:102394328-102394554 | Rare:63 | ||||
chr10:102432543-102432788 | Common:1; Rare:73 | ||||
chr10:102644914-102645108 | Rare:43 |