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 |
---|---|---|---|---|---|---|---|---|
chr14 | 95597047 | 95597064 | ZNF410 | JASPAR | yes | 107603770 | ||
chr14 | 95597049 | 95597054 | GATA2 | JASPAR | yes | 107603771 | ||
chr14 | 95597052 | 95597072 | RREB1 | JASPAR | yes | 107603772 | ||
chr14 | 95597055 | 95597059 | H1TF2 | TRANSFAC | yes | 107603773 | ||
chr14 | 95597055 | 95597059 | NFE | TRANSFAC | yes | 107603774 | ||
chr14 | 95597055 | 95597059 | SRF | TRANSFAC | yes | 107603775 | ||
chr14 | 95597060 | 95597080 | RREB1 | JASPAR | yes | 107603776 | ||
chr14 | 95597066 | 95597081 | RUNX2 | JASPAR | yes | 107603777 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr14 | 95597001 | rs575576382 | T | C | no | 3753215 | |
chr14 | 95597007 | rs147563150 | G | A | no | 3753216 | |
chr14 | 95597010 | rs374884911 | CTG | C | no | 3753217 | |
chr14 | 95597033 | rs73331543 | G | A | no | 3753218 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr14 | 95552565 | 95624347 | - | DICER1 | ENSG00000100697.10 | 95624347 | 0.7 | 0.98 | 13608 | 72735 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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