Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:7787958-7788263 | Common:1; Rare:123 | ||||
chr10:12068697-12068970 | Common:2; Rare:86 | ||||
chr10:12129458-12129719 | Rare:107 | ||||
chr10:12195809-12196248 | Rare:123 | ||||
chr10:13099943-13100273 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13300055-13300377 | Rare:85; Clinvar:1 | ||||
chr10:14838007-14838345 | Common:2; Rare:89 | ||||
chr10:14878627-14878884 | Common:2; Rare:78 | ||||
chr10:14954023-14954195 | Rare:61 | ||||
chr10:15097293-15097378 | Common:1; Rare:44 | ||||
chr10:15860279-15860589 | Common:2; Rare:87 | ||||
chr10:17228453-17228675 | Common:1; Rare:59 | ||||
chr10:17230510-17230710 | Rare:82; Clinvar:1 | ||||
chr10:17643871-17644241 | Common:2; Rare:112 | ||||
chr10:17809181-17809353 | Rare:16 |