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 |
|---|---|---|---|---|---|---|---|---|
| chr17 | 38496681 | 38496696 | TP53 | JASPAR | yes | 21234656 | ||
| chr17 | 38496681 | 38496696 | TP53 | JASPAR | yes | 54208045 | ||
| chr17 | 38496689 | 38496704 | FOXA1 | JASPAR | yes | 21234657 | ||
| chr17 | 38496689 | 38496704 | FOXA1 | JASPAR | yes | 54208046 | ||
| chr17 | 38496697 | 38496712 | PRDM1 | JASPAR | yes | 21234658 | ||
| chr17 | 38496697 | 38496712 | PRDM1 | JASPAR | yes | 54208047 | ||
| chr17 | 38496703 | 38496708 | ETS2 | TRANSFAC | yes | 21234659 | ||
| chr17 | 38496703 | 38496708 | ETS2 | TRANSFAC | yes | 54208048 | ||
| chr17 | 38496731 | 38496745 | TLX1 | JASPAR | yes | 21234660 | ||
| chr17 | 38496731 | 38496745 | TLX1 | JASPAR | yes | 54208049 | ||
| chr17 | 38496746 | 38496751 | ETS2 | TRANSFAC | yes | 21234661 | ||
| chr17 | 38496746 | 38496751 | ETS2 | TRANSFAC | yes | 54208050 | ||
| chr17 | 38496752 | 38496770 | RARA | JASPAR | yes | 21234662 | ||
| chr17 | 38496752 | 38496770 | RARA | JASPAR | yes | 54208051 | ||
| chr17 | 38496771 | 38496786 | TFAP2C | JASPAR | yes | 21234663 | ||
| chr17 | 38496771 | 38496786 | TFAP2C | JASPAR | yes | 54208052 | ||
| chr17 | 38496773 | 38496776 | MYB | TRANSFAC | yes | 21234664 | ||
| chr17 | 38496773 | 38496776 | MYB | TRANSFAC | yes | 54208053 | ||
| chr17 | 38496776 | 38496785 | TFAP2A | JASPAR | yes | 21234665 | ||
| chr17 | 38496776 | 38496785 | TFAP2A | JASPAR | yes | 54208054 | ||
| chr17 | 38496780 | 38496795 | HNF4A | JASPAR | yes | 21234666 | ||
| chr17 | 38496780 | 38496795 | HNF4A | JASPAR | yes | 54208055 | ||
| chr17 | 38496781 | 38496795 | NR2F1 | JASPAR | yes | 21234667 | ||
| chr17 | 38496781 | 38496795 | NR2F1 | JASPAR | yes | 54208056 | ||
| chr17 | 38496781 | 38496796 | HNF4G | JASPAR | yes | 21234668 | ||
| chr17 | 38496781 | 38496796 | HNF4G | JASPAR | yes | 54208057 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 38496752 | rs59406133 | T | A |
|
4866350 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 38443885 | 38459171 | + | CDC6 | ENSG00000094804.5 | 38443885 | 0.9 | 0.99 | 15763 | 47233 | |
| chr17 | 38465444 | 38513094 | + | RARA | ENSG00000131759.13 | 38465444 | 0.75 | 1.0 | 15764 | 68792 | |
| chr17 | 38516907 | 38520945 | + | CTD-2267D19.3 | ENSG00000266208.1 | 38516907 | 0.82 | 0.99 | 15765 | 79879 | |
| chr17 | 38517235 | 38520067 | - | GJD3 | ENSG00000183153.5 | 38520067 | 0.97 | 1.0 | 15766 | 76719 | |
| chr17 | 38544768 | 38574202 | - | TOP2A | ENSG00000131747.10 | 38574202 | 0.95 | 0.97 | 15767 | 22584 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|