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 |
|---|---|---|---|---|---|---|---|---|
| chr5 | 149266699 | 149266711 | FOXI1 | JASPAR | yes | 70737189 | ||
| chr5 | 149266701 | 149266712 | FOXH1 | JASPAR | yes | 70737190 | ||
| chr5 | 149266709 | 149266715 | SOX10 | JASPAR | yes | 70737191 | ||
| chr5 | 149266729 | 149266734 | GATA2 | JASPAR | yes | 70737192 | ||
| chr5 | 149266749 | 149266764 | PRDM1 | JASPAR | yes | 70737193 | ||
| chr5 | 149266749 | 149266767 | IRF2 | JASPAR | yes | 70737194 | ||
| chr5 | 149266750 | 149266762 | IRF1 | JASPAR | yes | 70737195 | ||
| chr5 | 149266761 | 149266766 | MYB | TRANSFAC | yes | 70737196 | ||
| chr5 | 149266781 | 149266790 | SOX9 | JASPAR | yes | 70737197 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr5 | 149266697 | rs529786439 | C | T | no | 8611776 | |
| chr5 | 149266716 | rs112349204 | A | G,T | no | 8611777 | |
| chr5 | 149266790 | rs182669690 | G | A |
|
8611778 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5 | 149237519 | 149324356 | - | PDE6A | ENSG00000132915.6 | 149324356 | 0.86 | 0.87 | 5869 | 42439 | |
| chr5 | 149340300 | 149373018 | + | SLC26A2 | ENSG00000155850.7 | 149340300 | 0.86 | 0.97 | 5870 | 26495 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|