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 |
|---|---|---|---|---|---|---|---|---|
| chr12 | 47294532 | 47294546 | POU1F1 | JASPAR | yes | 82396730 | ||
| chr12 | 47294533 | 47294545 | POU3F2 | JASPAR | yes | 82396731 | ||
| chr12 | 47294533 | 47294546 | POU3F3 | JASPAR | yes | 82396732 | ||
| chr12 | 47294539 | 47294544 | GATA2 | JASPAR | yes | 82396733 | ||
| chr12 | 47294554 | 47294562 | RHOXF1 | JASPAR | yes | 82396734 | ||
| chr12 | 47294555 | 47294565 | PAX3 | JASPAR | yes | 82396735 | ||
| chr12 | 47294555 | 47294565 | PAX7 | JASPAR | yes | 82396736 | ||
| chr12 | 47294560 | 47294564 | YY1 | TRANSFAC | yes | 82396737 | ||
| chr12 | 47294566 | 47294574 | RHOXF1 | JASPAR | yes | 82396738 | ||
| chr12 | 47294589 | 47294601 | GLI2 | JASPAR | yes | 82396739 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr12 | 47294517 | rs369632969 | A | T | no | 2607179 | |
| chr12 | 47294524 | rs151247799 | T | C | no | 2607180 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12 | 47158546 | 47226191 | - | SLC38A4 | ENSG00000139209.11 | 47226191 | 0.99 | 0.98 | 11977 | 31714 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|