Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:38702306-38702482 | Rare:62 | ||||
chr17:38719631-38719861 | Rare:89 | ||||
chr17:42422617-42422886 | Rare:110; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:43315653-43315934 | Common:7; Rare:128 | ||||
chr17:43388301-43388332 | Rare:7 | ||||
chr17:45149236-45149391 | Rare:51 | ||||
chr17:45149887-45150055 | Rare:34 | ||||
chr17:45585169-45585204 | Rare:2 | ||||
chr17:47100277-47100422 | Common:1; Rare:38 | ||||
chr17:50189368-50189733 | Rare:80; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr17:50189858-50190115 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr17:50197703-50197796 | Rare:26; Clinvar:3 | ||||
chr17:58324403-58324542 | Rare:42 | ||||
chr17:64145768-64145975 | Common:2; Rare:51 | ||||
chr17:64329702-64329810 | Common:3; Rare:24 |