Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
| Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
|---|---|---|---|---|---|---|---|---|
| chr16 | 29709885 | 29709898 | NR2F1 | JASPAR | yes | 49364005 | ||
| chr16 | 29709896 | 29709906 | MLXIPL | JASPAR | yes | 49364006 | ||
| chr16 | 29709896 | 29709906 | MLX | JASPAR | yes | 49364007 | ||
| chr16 | 29709898 | 29709903 | MYC | TRANSFAC | yes | 49364008 | ||
| chr16 | 29709898 | 29709903 | USF1 | TRANSFAC | yes | 49364009 | ||
| chr16 | 29709898 | 29709903 | USF2 | TRANSFAC | yes | 49364010 | ||
| chr16 | 29709898 | 29709905 | USF1 | JASPAR | yes | 49364011 | ||
| chr16 | 29709940 | 29709954 | IRF7 | JASPAR | yes | 10276081 | ||
| chr16 | 29709940 | 29709954 | IRF8 | JASPAR | yes | 10276082 | ||
| chr16 | 29709940 | 29709954 | IRF7 | JASPAR | yes | 49364012 | ||
| chr16 | 29709940 | 29709954 | IRF8 | JASPAR | yes | 49364013 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16 | 29674300 | 29682187 | + | SPN | ENSG00000197471.7 | 29674300 | 0.92 | 0.99 | 14706 | 64447 | |
| chr16 | 29674600 | 29710020 | + | QPRT | ENSG00000103485.13 | 29674600 | 0.86 | 0.95 | 14707 | 64747 | |
| chr16 | 29753784 | 29757327 | - | C16orf54 | ENSG00000185905.3 | 29757327 | 0.97 | 0.96 | 14708 | 52642 | |
| chr16 | 29789561 | 29793096 | + | ZG16 | ENSG00000174992.6 | 29789561 | 1.0 | 0.97 | 14709 | 20408 | |
| chr16 | 29802040 | 29816706 | + | KIF22 | ENSG00000079616.8 | 29802040 | 0.83 | 1.0 | 14710 | 7929 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|