Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:32315881-32316081 | Common:1; Rare:41; Clinvar (benign):2 | ||||
chr13:32428075-32428194 | Rare:28 | ||||
chr13:33205939-33206235 | Rare:65 | ||||
chr13:33285634-33285861 | Common:1; Rare:52 | ||||
chr13:34942160-34942298 | Common:3; Rare:39 | ||||
chr13:35476651-35476809 | Common:1; Rare:24 | ||||
chr13:36345538-36345657 | Common:1; Rare:23 | ||||
chr13:36346079-36346477 | Common:4; Rare:98; Clinvar:2; Clinvar (benign):3 | ||||
chr13:36346614-36346821 | Common:4; Rare:61 | ||||
chr13:37000756-37000815 | Rare:29; Clinvar (pathogenic):1 | ||||
chr13:37059585-37059751 | Common:1; Rare:55 | ||||
chr13:38350215-38350281 | Rare:34 | ||||
chr13:39038094-39038495 | Common:1; Rare:97 | ||||
chr13:39655633-39655802 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr13:40771100-40771344 | Common:3; Rare:85 |