Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7583665-7583858 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
chr17:10697503-10697646 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069470-14069523 | Common:1; Rare:20; Clinvar (benign):2 | ||||
chr17:17591659-17591891 | Common:1; Rare:65 | ||||
chr17:18314964-18315283 | Rare:94 | ||||
chr17:27293958-27294115 | Common:1; Rare:65 | ||||
chr17:28335425-28335785 | Common:1; Rare:83 | ||||
chr17:28598994-28599153 | Common:2; Rare:44 | ||||
chr17:28661888-28662297 | Common:1; Rare:143 | ||||
chr17:32350014-32350184 | Rare:85 | ||||
chr17:41812645-41813022 | Common:2; Rare:87; Clinvar:5 | ||||
chr17:42017405-42017576 | Common:1; Rare:57 | ||||
chr17:43125354-43125580 | Rare:38; Clinvar:3; Clinvar (benign):2 | ||||
chr17:44899419-44899756 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45061012-45061323 | Common:2; Rare:82 |