Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:97222185-97222415 | Rare:37 | ||||
chr13:97433949-97434166 | Common:1; Rare:81 | ||||
chr13:98576172-98576264 | Rare:30 | ||||
chr13:99086619-99086799 | Common:2; Rare:74 | ||||
chr13:99200663-99200921 | Common:6; Rare:120 | ||||
chr13:99307364-99307420 | Rare:8 | ||||
chr13:99606475-99606698 | Common:6; Rare:66 | ||||
chr13:100088868-100089134 | Rare:100; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674774-100675155 | Common:4; Rare:158 | ||||
chr13:102402351-102402475 | Rare:26 | ||||
chr13:102596785-102597045 | Common:1; Rare:123; Clinvar (benign):1 | ||||
chr13:102773699-102773860 | Rare:66 | ||||
chr13:102798961-102799357 | Rare:79 | ||||
chr13:102845707-102846168 | Common:9; Rare:117; Clinvar:4; Clinvar (benign):4 | ||||
chr13:102846197-102846314 | Rare:42; Clinvar:1 |