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 | 60557254 | 60557258 | LFA1 | TRANSFAC | yes | 21269895 | ||
chr17 | 60557259 | 60557263 | LFA1 | TRANSFAC | yes | 21269896 | ||
chr17 | 60557270 | 60557278 | EHF | JASPAR | yes | 21269897 | ||
chr17 | 60557273 | 60557287 | PLAG1 | JASPAR | yes | 21269898 | ||
chr17 | 60557297 | 60557318 | IRF1 | JASPAR | yes | 21269899 | ||
chr17 | 60557300 | 60557314 | STAT1 | JASPAR | yes | 21269900 | ||
chr17 | 60557301 | 60557322 | IRF1 | JASPAR | yes | 21269901 | ||
chr17 | 60557302 | 60557323 | ZNF263 | JASPAR | yes | 21269902 | ||
chr17 | 60557303 | 60557318 | STAT2 | JASPAR | yes | 21269903 | ||
chr17 | 60557305 | 60557326 | ZNF263 | JASPAR | yes | 21269904 | ||
chr17 | 60557306 | 60557321 | FOXP1 | JASPAR | yes | 21269905 | ||
chr17 | 60557313 | 60557318 | ETS2 | TRANSFAC | yes | 21269906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
chr17 | 60501228 | 60527454 | + | METTL2A | ENSG00000087995.11 | 60501228 | 0.68 | 1.0 | 16128 | 43976 | |
chr17 | 60536019 | 60692842 | + | TLK2 | ENSG00000146872.13 | 60536019 | 0.69 | 0.99 | 16129 | 78767 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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