Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:100088890-100089134 | Rare:88; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674774-100675060 | Common:3; Rare:117 | ||||
chr13:102596785-102597059 | Common:1; Rare:127; Clinvar (benign):1 | ||||
chr13:102773740-102773842 | Rare:51 | ||||
chr13:102798950-102799124 | Common:1; Rare:37 | ||||
chr13:102845695-102846167 | Common:9; Rare:124; Clinvar:4; Clinvar (benign):4 | ||||
chr13:106567919-106568267 | Rare:94 | ||||
chr13:108218313-108218520 | Rare:80 | ||||
chr13:110561668-110561893 | Common:5; Rare:79 | ||||
chr13:110615397-110615671 | Common:2; Rare:96 | ||||
chr13:110712436-110712535 | Rare:46 | ||||
chr13:110713008-110713267 | Common:2; Rare:116 | ||||
chr13:110713487-110713657 | Common:2; Rare:73 | ||||
chr13:110715341-110715569 | Common:1; Rare:91 | ||||
chr13:110715803-110715889 | Rare:63 |