Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053336-96053526 | Common:2; Rare:88 | ||||
chr13:97222128-97222402 | Rare:52 | ||||
chr13:98752609-98752793 | Common:3; Rare:43 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088936-100089120 | Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597035 | Common:1; Rare:119 | ||||
chr13:102798962-102799124 | Rare:34 | ||||
chr13:102845734-102846106 | Common:8; Rare:98; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567703-106567731 | Rare:5 | ||||
chr13:108218321-108218520 | Rare:78 | ||||
chr13:110307155-110307421 | Common:4; Rare:88; Clinvar (benign):4 | ||||
chr13:110561664-110561893 | Common:5; Rare:81 | ||||
chr13:110615415-110615610 | Common:1; Rare:67 | ||||
chr13:110713018-110713266 | Common:2; Rare:108 | ||||
chr13:111153552-111153721 | Common:2; Rare:82 |