Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:5097737-5098007 | Common:4; Rare:98 | ||||
chr16:8797631-8797872 | Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11851499-11851660 | Rare:81 | ||||
chr16:11915937-11916135 | Common:1; Rare:74 | ||||
chr16:11976477-11976734 | Common:5; Rare:94 | ||||
chr16:14071260-14071345 | Rare:27 | ||||
chr16:14632729-14632983 | Common:1; Rare:84 | ||||
chr16:15643048-15643284 | Common:1; Rare:83; Clinvar:1 | ||||
chr16:18801501-18801865 | Common:4; Rare:124 | ||||
chr16:20806435-20806542 | Rare:43 | ||||
chr16:21953028-21953405 | Common:1; Rare:94; Clinvar (benign):3 | ||||
chr16:22436942-22437028 | Rare:34 | ||||
chr16:23453163-23453268 | Rare:32 | ||||
chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24729607-24729727 | Common:6; Rare:67 |