Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15999616-15999981 | Common:3; Rare:168; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:17281183-17281376 | Rare:77 | ||||
chr17:17496388-17496580 | Common:2; Rare:51 | ||||
chr17:18314944-18315308 | Rare:104 | ||||
chr17:18781088-18781294 | Common:5; Rare:57 | ||||
chr17:18856165-18856362 | Common:1; Rare:36 | ||||
chr17:19648626-19648955 | Common:3; Rare:110 | ||||
chr17:21214148-21214322 | Common:2; Rare:73 | ||||
chr17:27293954-27294122 | Common:1; Rare:72 | ||||
chr17:28335420-28335810 | Common:1; Rare:89 | ||||
chr17:28357451-28357655 | Common:5; Rare:101 | ||||
chr17:28599007-28599170 | Common:2; Rare:43 | ||||
chr17:28645106-28645348 | Common:1; Rare:93 | ||||
chr17:28661876-28662297 | Common:1; Rare:151 | ||||
chr17:28717804-28717995 | Rare:42 |