Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18087773-18087991 | Rare:57 | ||||
chr17:18183756-18183925 | Rare:73 | ||||
chr17:18314944-18315293 | Rare:103 | ||||
chr17:18781081-18781316 | Common:5; Rare:66 | ||||
chr17:18856161-18856358 | Common:1; Rare:36 | ||||
chr17:19362572-19362773 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
chr17:19378201-19378499 | Common:1; Rare:69 | ||||
chr17:19648502-19648967 | Common:4; Rare:146 | ||||
chr17:21214139-21214359 | Common:2; Rare:98 | ||||
chr17:27293981-27294124 | Common:1; Rare:59 | ||||
chr17:28318904-28319213 | Common:3; Rare:102 | ||||
chr17:28335425-28335810 | Common:1; Rare:87 | ||||
chr17:28357455-28357667 | Common:5; Rare:105 | ||||
chr17:28384555-28384608 | Rare:24 | ||||
chr17:28661881-28662256 | Common:1; Rare:133 |