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 |
---|---|---|---|---|---|---|---|---|
chr16 | 70427698 | 70427708 | TEAD1 | JASPAR | yes | 49388720 | ||
chr16 | 70427698 | 70427708 | TEAD4 | JASPAR | yes | 49388721 | ||
chr16 | 70427699 | 70427707 | TEAD3 | JASPAR | yes | 49388722 | ||
chr16 | 70427734 | 70427753 | RFX2 | JASPAR | yes | 49388723 | ||
chr16 | 70427736 | 70427751 | RFX5 | JASPAR | yes | 49388724 | ||
chr16 | 70427738 | 70427754 | RFX2 | JASPAR | yes | 49388725 | ||
chr16 | 70427738 | 70427754 | RFX3 | JASPAR | yes | 49388726 | ||
chr16 | 70427738 | 70427754 | RFX4 | JASPAR | yes | 49388727 | ||
chr16 | 70427738 | 70427754 | RFX5 | JASPAR | yes | 49388728 | ||
chr16 | 70427739 | 70427758 | RFX2 | JASPAR | yes | 49388729 | ||
chr16 | 70427769 | 70427775 | SOX10 | JASPAR | yes | 49388730 | ||
chr16 | 70427776 | 70427784 | EHF | JASPAR | yes | 49388731 | ||
chr16 | 70427778 | 70427783 | ETS2 | TRANSFAC | yes | 49388732 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
chr16 | 70333097 | 70400163 | + | RP11-529K1.3 | ENSG00000260537.1 | 70333097 | 0.92 | 0.87 | 15023 | 5400 | |
chr16 | 70380732 | 70407286 | + | DDX19A | ENSG00000168872.11 | 70380732 | 0.56 | 0.99 | 15024 | 53035 | |
chr16 | 70413338 | 70473140 | - | ST3GAL2 | ENSG00000157350.8 | 70473140 | 0.67 | 0.99 | 15025 | 54655 | |
chr16 | 70488324 | 70514177 | + | FUK | ENSG00000157353.12 | 70488324 | 0.65 | 1.0 | 15026 | 39471 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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