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 |
|---|
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr18 | 679561 | rs35144608 | GA | G | no | 5132690 | |
| chr18 | 679561 | rs548108090 | GA | G | no | 5132691 | |
| chr18 | 679561 | rs60703222 | GA | G | no | 5132692 | |
| chr18 | 679561 | rs71363251 | GAA | G,GA | no | 5132693 | |
| chr18 | 679561 | rs869134611 | GAA | G | no | 5132694 | |
| chr18 | 679564 | rs571673558 | A | T | no | 5132695 | |
| chr18 | 679566 | rs545583690 | A | G | no | 5132696 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18 | 580367 | 581524 | + | CETN1 | ENSG00000177143.3 | 580367 | 0.96 | 1.0 | 16412 | 808 | |
| chr18 | 596988 | 650334 | + | CLUL1 | ENSG00000079101.12 | 596988 | 0.94 | 0.98 | 16413 | 17429 | |
| chr18 | 641320 | 658340 | - | C18orf56 | ENSG00000176912.3 | 658340 | 0.94 | 1.0 | 16414 | 78781 | |
| chr18 | 657604 | 673578 | + | TYMS | ENSG00000176890.11 | 657604 | 0.95 | 1.0 | 16415 | 78045 | |
| chr18 | 670324 | 712676 | - | ENOSF1 | ENSG00000132199.14 | 712676 | 0.76 | 1.0 | 16416 | 66892 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|