Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:53584-53845 | Common:6; Rare:84 | ||||
chr16:636270-636457 | Common:4; Rare:56 | ||||
chr16:1420734-1420969 | Common:1; Rare:94 | ||||
chr16:1943183-1943493 | Common:1; Rare:95 | ||||
chr16:2047806-2048024 | Rare:97; Clinvar:2 | ||||
chr16:2777240-2777373 | Common:1; Rare:52 | ||||
chr16:3134861-3135143 | Common:3; Rare:75 | ||||
chr16:3457908-3458069 | Common:2; Rare:77 | ||||
chr16:4425752-4425874 | Common:1; Rare:57 | ||||
chr16:4476286-4476459 | Common:2; Rare:65 | ||||
chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr16:14630188-14630405 | Rare:95 | ||||
chr16:23641247-23641523 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
chr16:23678634-23678874 | Common:3; Rare:56 | ||||
chr16:24729490-24729727 | Common:6; Rare:100 |