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 |
|---|---|---|---|---|---|---|---|---|
| chr17 | 9549833 | 9549840 | SPIB | JASPAR | yes | 21197645 | ||
| chr17 | 9549833 | 9549840 | SPIB | JASPAR | yes | 53058686 | ||
| chr17 | 9549833 | 9549844 | FLI1 | JASPAR | yes | 21197646 | ||
| chr17 | 9549833 | 9549844 | FLI1 | JASPAR | yes | 53058687 | ||
| chr17 | 9549834 | 9549842 | EHF | JASPAR | yes | 21197647 | ||
| chr17 | 9549834 | 9549842 | EHF | JASPAR | yes | 53058688 | ||
| chr17 | 9549862 | 9549874 | PBX1 | JASPAR | yes | 21197648 | ||
| chr17 | 9549862 | 9549874 | PBX1 | JASPAR | yes | 53058689 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 9549792 | rs112603294 | A | G | no | 4744337 | |
| chr17 | 9549815 | rs147762100 | T | C | no | 4744338 | |
| chr17 | 9549826 | rs189241769 | A | G | no | 4744339 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 9153788 | 9479908 | - | STX8 | ENSG00000170310.10 | 9479908 | 0.69 | 1.0 | 15430 | 30116 | |
| chr17 | 9479944 | 9546776 | + | WDR16 | ENSG00000166596.10 | 9479944 | 0.97 | 0.88 | 15431 | 30152 | |
| chr17 | 9548015 | 9633008 | + | USP43 | ENSG00000154914.12 | 9548015 | 0.81 | 1.0 | 15432 | 98223 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|