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 | 64963089 | 64963109 | TP63 | JASPAR | yes | 21278687 | ||
| chr17 | 64963090 | 64963108 | TP63 | JASPAR | yes | 21278688 | ||
| chr17 | 64963100 | 64963109 | SNAI2 | JASPAR | yes | 21278689 | ||
| chr17 | 64963104 | 64963113 | NFIX | JASPAR | yes | 21278690 | ||
| chr17 | 64963104 | 64963114 | NFIA | JASPAR | yes | 21278691 | ||
| chr17 | 64963105 | 64963114 | HIC2 | JASPAR | yes | 21278692 | ||
| chr17 | 64963106 | 64963112 | NFIC | JASPAR | yes | 21278693 | ||
| chr17 | 64963130 | 64963141 | NFE2 | JASPAR | yes | 21278694 | ||
| chr17 | 64963131 | 64963140 | JDP2 | JASPAR | yes | 21278695 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 64963128 | rs185936902 | A | G | no | 5002003 |
| 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 | 64961026 | 65029514 | + | CACNG4 | ENSG00000075461.5 | 64961026 | 0.95 | 0.91 | 16173 | 97962 | |
| chr17 | 65027509 | 65028198 | + | AC005544.1 | ENSG00000214167.1 | 65027509 | 0.97 | 1.0 | 16174 | 35670 | |
| chr17 | 65040706 | 65052909 | + | CACNG1 | ENSG00000108878.3 | 65040706 | 0.97 | 1.0 | 16175 | 22473 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|