Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:88686463-88686789 | Common:3; Rare:105 | ||||
chr16:88856873-88857166 | Common:4; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
chr16:89217619-89217743 | Common:1; Rare:58 | ||||
chr16:89560573-89560725 | Rare:67 | ||||
chr16:89657644-89658091 | Common:3; Rare:235 | ||||
chr16:89686560-89686950 | Common:10; Rare:197 | ||||
chr16:89720865-89720993 | Common:1; Rare:34 | ||||
chr16:89816611-89816769 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr16:89972478-89972648 | Common:1; Rare:64 | ||||
chr16:90022581-90022713 | Rare:53 | ||||
chr17:331030-331193 | Common:7; Rare:38 | ||||
chr17:352506-352623 | Common:2; Rare:28 | ||||
chr17:352760-353029 | Common:3; Rare:53 | ||||
chr17:714777-714899 | Common:2; Rare:40 | ||||
chr17:752146-752303 | Common:2; Rare:67 |