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 |
|---|---|---|---|---|---|---|---|---|
| chr1 | 51779025 | 51779033 | FOXO3 | JASPAR | yes | 28836657 | ||
| chr1 | 51779025 | 51779033 | FOXO3 | JASPAR | yes | 118289177 | ||
| chr1 | 51779037 | 51779047 | SP1 | JASPAR | yes | 28836658 | ||
| chr1 | 51779037 | 51779047 | SP1 | JASPAR | yes | 118289178 | ||
| chr1 | 51779041 | 51779055 | PLAG1 | JASPAR | yes | 28836659 | ||
| chr1 | 51779041 | 51779055 | PLAG1 | JASPAR | yes | 118289179 | ||
| chr1 | 51779051 | 51779056 | SP1 | TRANSFAC | yes | 28836660 | ||
| chr1 | 51779051 | 51779056 | SP1 | TRANSFAC | yes | 118289180 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr1 | 51779053 | rs189315815 | C | T |
|
305085 | |
| chr1 | 51779056 | rs55763623 | C | A,G |
|
305086 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1 | 51701943 | 51739127 | + | RNF11 | ENSG00000123091.4 | 51701943 | 0.61 | 0.99 | 687 | 22915 | |
| chr1 | 51752930 | 51810788 | - | TTC39A | ENSG00000085831.11 | 51810788 | 0.84 | 1.0 | 688 | 68297 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|