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 |
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chr17 | 32636678 | 32636692 | STAT1 | JASPAR | yes | 21223630 | ||
chr17 | 32636678 | 32636693 | PRDM1 | JASPAR | yes | 21223631 | ||
chr17 | 32636678 | 32636693 | STAT2 | JASPAR | yes | 21223632 | ||
chr17 | 32636678 | 32636696 | IRF2 | JASPAR | yes | 21223633 | ||
chr17 | 32636679 | 32636691 | IRF1 | JASPAR | yes | 21223634 | ||
chr17 | 32636703 | 32636719 | SOX4 | JASPAR | yes | 21223635 | ||
chr17 | 32636707 | 32636725 | NFYA | JASPAR | yes | 21223636 | ||
chr17 | 32636719 | 32636723 | H4TF2 | TRANSFAC | yes | 21223637 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
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Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
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chr17 | 32581900 | 32582306 | - | AC005549.3 | ENSG00000268024.1 | 32582306 | 1.0 | 0.0 | 15642 | 45628 | |
chr17 | 32582304 | 32584222 | + | CCL2 | ENSG00000108691.5 | 32582304 | 0.83 | 0.97 | 15643 | 45626 | |
chr17 | 32597240 | 32599261 | + | CCL7 | ENSG00000108688.7 | 32597240 | 0.99 | 0.99 | 15644 | 60562 | |
chr17 | 32612687 | 32615353 | + | CCL11 | ENSG00000172156.3 | 32612687 | 0.96 | 1.0 | 15645 | 76009 | |
chr17 | 32646055 | 32648421 | + | CCL8 | ENSG00000108700.4 | 32646055 | 0.83 | 0.0 | 15646 | 90688 | |
chr17 | 32683471 | 32685629 | + | CCL13 | ENSG00000181374.3 | 32683471 | 0.9 | 0.0 | 15647 | 53272 | |
chr17 | 32687347 | 32690250 | - | CCL1 | ENSG00000108702.3 | 32690250 | 1.0 | 0.0 | 15648 | 46493 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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