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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chr11 | 125340433 | 125340438 | GATA2 | JASPAR | yes | 114151035 | ||
chr11 | 125340441 | 125340452 | CDX2 | JASPAR | yes | 114151036 | ||
chr11 | 125340441 | 125340455 | FOXF2 | JASPAR | yes | 114151037 | ||
chr11 | 125340446 | 125340454 | FOXG1 | JASPAR | yes | 114151038 | ||
chr11 | 125340446 | 125340454 | FOXO3 | JASPAR | yes | 114151039 | ||
chr11 | 125340479 | 125340483 | H1TF2 | TRANSFAC | yes | 114151040 | ||
chr11 | 125340479 | 125340483 | NFE | TRANSFAC | yes | 114151041 | ||
chr11 | 125340479 | 125340483 | SRF | TRANSFAC | yes | 114151042 |
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 | 125315646 | 125366213 | - | FEZ1 | ENSG00000149557.8 | 125366213 | 0.96 | 0.99 | 11602 | 74273 | |
chr11 | 125365110 | 125369424 | + | AP000708.1 | ENSG00000255537.1 | 125365110 | 0.86 | 0.93 | 11603 | 75376 | |
chr11 | 125439112 | 125454575 | + | EI24 | ENSG00000149547.10 | 125439112 | 0.79 | 0.99 | 11604 | 1374 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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