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 |
---|---|---|---|---|---|---|---|---|
chr1 | 11525460 | 11525464 | H1TF2 | TRANSFAC | yes | 118230289 | ||
chr1 | 11525460 | 11525464 | NFE | TRANSFAC | yes | 118230290 | ||
chr1 | 11525460 | 11525464 | SRF | TRANSFAC | yes | 118230291 | ||
chr1 | 11525471 | 11525475 | H4TF2 | TRANSFAC | yes | 118230292 | ||
chr1 | 11525477 | 11525497 | TP53 | JASPAR | yes | 118230293 | ||
chr1 | 11525499 | 11525503 | H4TF2 | TRANSFAC | yes | 118230294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
chr1 | 11539223 | 11597641 | + | PTCHD2 | ENSG00000204624.6 | 11539223 | 0.89 | 1.0 | 150 | 86302 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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