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 | 117375657 | 117375672 | FOXP1 | JASPAR | yes | 82484714 | ||
| chr12 | 117375657 | 117375672 | FOXP1 | JASPAR | yes | 124034893 | ||
| chr12 | 117375658 | 117375673 | FOXP1 | JASPAR | yes | 82484715 | ||
| chr12 | 117375658 | 117375673 | FOXP1 | JASPAR | yes | 124034894 | ||
| chr12 | 117375665 | 117375675 | HOXA13 | JASPAR | yes | 82484716 | ||
| chr12 | 117375665 | 117375675 | HOXA13 | JASPAR | yes | 124034895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12 | 117293949 | 117319246 | - | HRK | ENSG00000135116.5 | 117319246 | 0.98 | 1.0 | 12577 | 43581 | |
| chr12 | 117348761 | 117468953 | + | FBXW8 | ENSG00000174989.8 | 117348761 | 0.68 | 1.0 | 12578 | 73096 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|