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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chr14 | 89707920 | 89707935 | HSF1 | JASPAR | yes | 107593684 | ||
chr14 | 89707920 | 89707935 | HSF1 | JASPAR | yes | 117145476 | ||
chr14 | 89707921 | 89707934 | HSF4 | JASPAR | yes | 107593685 | ||
chr14 | 89707921 | 89707934 | HSF4 | JASPAR | yes | 117145477 | ||
chr14 | 89707922 | 89707937 | IRF9 | JASPAR | yes | 107593686 | ||
chr14 | 89707922 | 89707937 | IRF9 | JASPAR | yes | 117145478 | ||
chr14 | 89707924 | 89707938 | STAT1 | JASPAR | yes | 107593687 | ||
chr14 | 89707924 | 89707938 | STAT1 | JASPAR | yes | 117145479 |
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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Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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