Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27424562-27424732 | Common:2; Rare:55 | ||||
chr13:27450124-27450212 | Common:2; Rare:25 | ||||
chr13:28659066-28659181 | Rare:50; Clinvar (pathogenic):1 | ||||
chr13:30306959-30307197 | Common:5; Rare:57 | ||||
chr13:30465795-30466111 | Common:1; Rare:103 | ||||
chr13:30617588-30618000 | Common:1; Rare:127 | ||||
chr13:32315343-32315558 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
chr13:33285703-33285913 | Rare:49 | ||||
chr13:36346294-36346510 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
chr13:37000700-37000805 | Rare:42 | ||||
chr13:37059585-37059745 | Common:1; Rare:53 | ||||
chr13:37869759-37869930 | Common:1; Rare:39 | ||||
chr13:38349548-38349911 | Common:3; Rare:122; Clinvar (pathogenic):1 | ||||
chr13:39038067-39038426 | Common:1; Rare:91 | ||||
chr13:40771138-40771440 | Common:3; Rare:89 |