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 | 1793824 | 1793833 | VENTX | JASPAR | yes | 26208462 | ||
chr1 | 1793824 | 1793833 | VENTX | JASPAR | yes | 118215449 | ||
chr1 | 1793824 | 1793834 | GSX2 | JASPAR | yes | 26208463 | ||
chr1 | 1793824 | 1793834 | GSX2 | JASPAR | yes | 118215450 | ||
chr1 | 1793825 | 1793833 | BSX | JASPAR | yes | 26208464 | ||
chr1 | 1793825 | 1793833 | BSX | JASPAR | yes | 118215451 | ||
chr1 | 1793827 | 1793831 | YY1 | TRANSFAC | yes | 26208465 | ||
chr1 | 1793827 | 1793831 | YY1 | TRANSFAC | yes | 118215452 | ||
chr1 | 1793830 | 1793833 | MYB | TRANSFAC | yes | 26208466 | ||
chr1 | 1793830 | 1793833 | MYB | TRANSFAC | yes | 118215453 | ||
chr1 | 1793837 | 1793843 | MZF1 | JASPAR | yes | 26208467 | ||
chr1 | 1793837 | 1793843 | MZF1 | JASPAR | yes | 118215454 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr1 | 1793844 | rs58775734 | C | T | no | 9478 |
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 | 1682671 | 1711896 | - | NADK | ENSG00000008130.11 | 1711896 | 0.71 | 1.0 | 51 | 18067 | |
chr1 | 1716729 | 1822495 | - | GNB1 | ENSG00000078369.13 | 1822495 | 0.7 | 1.0 | 52 | 71367 | |
chr1 | 1846266 | 1848735 | + | CALML6 | ENSG00000169885.5 | 1846266 | 0.87 | 1.0 | 53 | 47596 | |
chr1 | 1849029 | 1850712 | - | TMEM52 | ENSG00000178821.8 | 1850712 | 0.99 | 1.0 | 54 | 43150 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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