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 | 9772002 | 9772012 | ETV6 | JASPAR | yes | 21197845 | ||
| chr17 | 9772003 | 9772011 | EHF | JASPAR | yes | 21197846 | ||
| chr17 | 9772004 | 9772011 | SPI1 | JASPAR | yes | 21197847 | ||
| chr17 | 9772042 | 9772046 | YY1 | TRANSFAC | yes | 21197848 | ||
| chr17 | 9772081 | 9772092 | FOXH1 | JASPAR | yes | 21197849 | ||
| chr17 | 9772082 | 9772088 | JUN | TRANSFAC | yes | 21197850 | ||
| chr17 | 9772082 | 9772093 | FOXC1 | JASPAR | yes | 21197851 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 9772011 | rs62066047 | T | A |
|
4745670 | |
| chr17 | 9772097 | rs369452885 | TC | T | no | 4745671 |
| 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 | 9674751 | 9694614 | - | DHRS7C | ENSG00000184544.7 | 9694614 | 1.0 | 0.0 | 15433 | 22612 | |
| chr17 | 9694544 | 9725388 | - | RP11-477N12.3 | ENSG00000214978.6 | 9725388 | 0.0 | 0.91 | 15434 | 53386 | |
| chr17 | 9725523 | 9795419 | + | GLP2R | ENSG00000065325.8 | 9725523 | 0.94 | 0.98 | 15435 | 53521 | |
| chr17 | 9799637 | 9808938 | - | RCVRN | ENSG00000109047.7 | 9808938 | 0.83 | 1.0 | 15436 | 63163 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|