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 | 87428039 | 87428399 | CTCF | UCSC Txn Factor | no | Conserved | 108219243 | |
chr16 | 87428150 | 87428165 | FOXP1 | JASPAR | yes | 49414141 | ||
chr16 | 87428154 | 87428162 | FOXO3 | JASPAR | yes | 49414142 | ||
chr16 | 87428165 | 87428173 | EHF | JASPAR | yes | 49414143 | ||
chr16 | 87428167 | 87428172 | ETS2 | TRANSFAC | yes | 49414144 | ||
chr16 | 87428170 | 87428189 | RFX2 | JASPAR | yes | 49414145 | ||
chr16 | 87428174 | 87428190 | RFX2 | JASPAR | yes | 49414146 | ||
chr16 | 87428174 | 87428190 | RFX3 | JASPAR | yes | 49414147 | ||
chr16 | 87428174 | 87428190 | RFX4 | JASPAR | yes | 49414148 | ||
chr16 | 87428174 | 87428190 | RFX5 | JASPAR | yes | 49414149 | ||
chr16 | 87428191 | 87428196 | SP1 | TRANSFAC | yes | 49414150 | ||
chr16 | 87428194 | 87428199 | SP1 | TRANSFAC | yes | 49414151 |
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 | 87117168 | 87351022 | - | C16orf95 | ENSG00000260456.2 | 87351022 | 0.91 | 0.99 | 15141 | 22908 | |
chr16 | 87336482 | 87367879 | - | RP11-178L8.4 | ENSG00000131152.4 | 87367879 | 0.86 | 0.78 | 15142 | 39765 | |
chr16 | 87360593 | 87425748 | - | FBXO31 | ENSG00000103264.11 | 87425748 | 0.64 | 1.0 | 15143 | 97634 | |
chr16 | 87417601 | 87438385 | + | MAP1LC3B | ENSG00000140941.8 | 87417601 | 0.61 | 1.0 | 15144 | 89487 | |
chr16 | 87439852 | 87525651 | - | ZCCHC14 | ENSG00000140948.7 | 87525651 | 0.7 | 1.0 | 15145 | 2558 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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