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 | 69060347 | 69060352 | ETS2 | TRANSFAC | yes | 49387440 | ||
chr16 | 69060347 | 69060355 | EHF | JASPAR | yes | 49387441 | ||
chr16 | 69060356 | 69060360 | NFE | TRANSFAC | yes | 49387442 | ||
chr16 | 69060356 | 69060361 | GATA1 | TRANSFAC | yes | 49387443 | ||
chr16 | 69060356 | 69060362 | GATA3 | JASPAR | yes | 49387444 | ||
chr16 | 69060364 | 69060376 | YY1 | JASPAR | yes | 49387445 | ||
chr16 | 69060369 | 69060373 | YY1 | TRANSFAC | yes | 49387446 | ||
chr16 | 69060388 | 69060403 | RUNX2 | JASPAR | yes | 49387447 | ||
chr16 | 69060399 | 69060411 | HLF | JASPAR | yes | 49387448 | ||
chr16 | 69060399 | 69060414 | JUND | JASPAR | yes | 49387449 | ||
chr16 | 69060421 | 69060439 | TP73 | JASPAR | yes | 49387450 | ||
chr16 | 69060425 | 69060429 | ESR1 | TRANSFAC | yes | 49387451 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr16 | 69060344 | rs372192316 | C | G,T | no | 4503833 | |
chr16 | 69060437 | rs181182144 | G | A |
|
4503834 |
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 | 69139467 | 69152622 | + | HAS3 | ENSG00000103044.6 | 69139467 | 0.98 | 1.0 | 14995 | 21014 | |
chr16 | 69152757 | 69154331 | - | CHTF8 | ENSG00000263203.1 | 69154331 | 0.86 | 0.79 | 14997 | 6150 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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