Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:74368122-74368385 | Common:1; Rare:72 | ||||
chr16:79598316-79598573 | Common:4; Rare:46 | ||||
chr16:79598778-79598813 | Rare:3 | ||||
chr16:79770505-79770726 | Common:5; Rare:96 | ||||
chr16:88765015-88765250 | Common:2; Rare:58 | ||||
chr17:7311045-7311481 | Rare:105 | ||||
chr17:7354482-7354563 | Common:2; Rare:18 | ||||
chr17:7916238-7916486 | Common:1; Rare:61 | ||||
chr17:8080655-8080895 | Common:2; Rare:76; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr17:8150081-8150237 | Rare:51 | ||||
chr17:8154427-8154541 | Rare:28 | ||||
chr17:8190136-8190229 | Rare:30 | ||||
chr17:8222535-8222676 | Common:2; Rare:31 | ||||
chr17:10803942-10803968 | Rare:5 | ||||
chr17:17836154-17836426 | Common:3; Rare:69 |