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 |
---|---|---|---|---|---|---|---|---|
chr11 | 124111956 | 124111969 | HSF1 | JASPAR | yes | 114149315 | ||
chr11 | 124111956 | 124111969 | HSF2 | JASPAR | yes | 114149316 | ||
chr11 | 124111956 | 124111969 | HSF4 | JASPAR | yes | 114149317 | ||
chr11 | 124111961 | 124111974 | HSF2 | JASPAR | yes | 114149318 | ||
chr11 | 124111971 | 124111991 | PPARG | JASPAR | yes | 114149319 | ||
chr11 | 124111990 | 124112005 | SOX21 | JASPAR | yes | 114149320 | ||
chr11 | 124111998 | 124112002 | YY1 | TRANSFAC | yes | 114149321 | ||
chr11 | 124112008 | 124112021 | ELF1 | JASPAR | yes | 114149322 | ||
chr11 | 124112021 | 124112031 | TEAD1 | JASPAR | yes | 114149323 | ||
chr11 | 124112021 | 124112031 | TEAD4 | JASPAR | yes | 114149324 | ||
chr11 | 124112021 | 124112033 | TEAD1 | JASPAR | yes | 114149325 | ||
chr11 | 124112022 | 124112030 | TEAD3 | JASPAR | yes | 114149326 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
chr11 | 124055923 | 124056952 | + | OR10D3 | ENSG00000197309.2 | 124055923 | 1.0 | 0.96 | 11575 | 44003 | |
chr11 | 124134723 | 124135763 | + | OR8G5 | ENSG00000255298.2 | 124134723 | 0.97 | 0.97 | 11576 | 77315 | |
chr11 | 124179708 | 124180733 | - | OR8D1 | ENSG00000196341.2 | 124180733 | 0.0 | 0.86 | 11577 | 31305 | |
chr11 | 124189134 | 124190184 | - | OR8D2 | ENSG00000197263.2 | 124190184 | 0.0 | 0.0 | 11578 | 21854 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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