Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13348017-13348310 | Rare:94 | ||||
chr10:14838029-14838380 | Common:2; Rare:95 | ||||
chr10:14878606-14878882 | Common:2; Rare:88 | ||||
chr10:14953977-14954179 | Rare:65; Clinvar (benign):1 | ||||
chr10:15097301-15097387 | Common:1; Rare:44 | ||||
chr10:15860320-15860583 | Common:1; Rare:68 | ||||
chr10:17228458-17228675 | Common:1; Rare:58 | ||||
chr10:17229022-17229026 | Rare:1 | ||||
chr10:17643894-17644286 | Common:2; Rare:116 | ||||
chr10:17808914-17809385 | Rare:74 | ||||
chr10:18651543-18651748 | Common:1; Rare:86 | ||||
chr10:18659250-18659573 | Common:2; Rare:105 | ||||
chr10:19816123-19816651 | Common:6; Rare:121 | ||||
chr10:21533996-21534354 | Common:3; Rare:143 | ||||
chr10:22316280-22316473 | Common:1; Rare:84 |