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 | 75756691 | 75756706 | FOXP1 | JASPAR | yes | 70665737 | ||
| chr5 | 75756692 | 75756707 | FOXP1 | JASPAR | yes | 70665738 | ||
| chr5 | 75756693 | 75756708 | FOXP1 | JASPAR | yes | 70665739 | ||
| chr5 | 75756694 | 75756709 | FOXP1 | JASPAR | yes | 70665740 | ||
| chr5 | 75756695 | 75756710 | FOXP1 | JASPAR | yes | 70665741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5 | 75699074 | 76003957 | + | IQGAP2 | ENSG00000145703.11 | 75699074 | 0.84 | 0.94 | 5470 | 42383 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|