Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102419678-102419799 | Rare:32 | ||||
chr10:102420765-102420893 | Rare:25 | ||||
chr10:102420970-102421247 | Rare:112 | ||||
chr10:102432530-102432788 | Common:1; Rare:78 | ||||
chr10:102461205-102461450 | Rare:68 | ||||
chr10:102502657-102503035 | Common:1; Rare:106 | ||||
chr10:102714182-102714671 | Common:2; Rare:156 | ||||
chr10:102743620-102744014 | Common:3; Rare:107 | ||||
chr10:102854124-102854292 | Common:1; Rare:61 | ||||
chr10:102854452-102854681 | Common:1; Rare:51 | ||||
chr10:102869402-102869766 | Common:9; Rare:89 | ||||
chr10:103193248-103193392 | Common:5; Rare:45; Clinvar (benign):1 | ||||
chr10:103276968-103277143 | Rare:46 | ||||
chr10:103350898-103351219 | Common:2; Rare:125 | ||||
chr10:103367815-103367989 | Common:3; Rare:32 |