Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:73058787-73059032 | Rare:88 | ||||
chr13:75549429-75549546 | Common:2; Rare:32 | ||||
chr13:76991969-76992206 | Common:3; Rare:109; Clinvar:20; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
chr13:77027144-77027298 | Common:5; Rare:48 | ||||
chr13:77535478-77535788 | Common:1; Rare:61 | ||||
chr13:78659121-78659235 | Common:2; Rare:83 | ||||
chr13:79405785-79405922 | Rare:50 | ||||
chr13:79406227-79406325 | Common:2; Rare:30 | ||||
chr13:79481049-79481479 | Common:2; Rare:173 | ||||
chr13:94596139-94596335 | Common:2; Rare:63 | ||||
chr13:95676884-95677227 | Common:3; Rare:129 | ||||
chr13:96053354-96053536 | Common:2; Rare:79 | ||||
chr13:97222154-97222397 | Rare:42 | ||||
chr13:98576172-98576280 | Common:1; Rare:34 | ||||
chr13:99200663-99200911 | Common:6; Rare:117 |