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 | 46986311 | 46986330 | PAX5 | JASPAR | yes | 28664143 | ||
chr1 | 46986311 | 46986330 | PAX5 | JASPAR | yes | 118286203 | ||
chr1 | 46986319 | 46986323 | NFE | TRANSFAC | yes | 28664144 | ||
chr1 | 46986319 | 46986323 | NFE | TRANSFAC | yes | 118286204 | ||
chr1 | 46986340 | 46986360 | RREB1 | JASPAR | yes | 28664145 | ||
chr1 | 46986340 | 46986360 | RREB1 | JASPAR | yes | 118286205 | ||
chr1 | 46986348 | 46986360 | INSM1 | JASPAR | yes | 28664146 | ||
chr1 | 46986348 | 46986360 | INSM1 | JASPAR | yes | 118286206 | ||
chr1 | 46986360 | 46986372 | TEAD1 | JASPAR | yes | 28664147 | ||
chr1 | 46986360 | 46986372 | TEAD1 | JASPAR | yes | 118286207 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr1 | 46986322 | rs1267313 | G | T |
|
289117 | |
chr1 | 46986372 | rs185371298 | C | T |
|
289118 |
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 | 46972668 | 46979898 | + | DMBX1 | ENSG00000197587.6 | 46972668 | 0.95 | 1.0 | 656 | 86347 | |
chr1 | 47011316 | 47017199 | - | KNCN | ENSG00000162456.5 | 47017199 | 0.99 | 0.0 | 657 | 69209 | |
chr1 | 47023090 | 47082515 | - | MKNK1 | ENSG00000079277.15 | 47082515 | 0.78 | 1.0 | 658 | 3893 | |
chr1 | 47073387 | 47082563 | - | MOB3C | ENSG00000142961.10 | 47082563 | 0.59 | 1.0 | 659 | 3845 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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