Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97687017-97687477 | Common:7; Rare:120 | ||||
chr10:98425659-98425874 | Common:1; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:99430616-99430965 | Common:3; Rare:85 | ||||
chr10:99659247-99659556 | Common:1; Rare:78 | ||||
chr10:99732072-99732329 | Rare:95; Clinvar:4 | ||||
chr10:100185918-100186165 | Rare:93 | ||||
chr10:100229553-100229640 | Rare:27 | ||||
chr10:100529817-100529968 | Rare:48 | ||||
chr10:100912663-100913028 | Common:1; Rare:108 | ||||
chr10:100913335-100913371 | Rare:13 | ||||
chr10:100969195-100969564 | Common:4; Rare:95 | ||||
chr10:100980538-100980951 | Common:3; Rare:133 | ||||
chr10:100987256-100987574 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996969-100997187 | Common:2; Rare:58 | ||||
chr10:101031093-101031533 | Common:1; Rare:101 |