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 |
---|---|---|---|---|---|---|---|---|
chr3 | 130841366 | 130841371 | SP1 | TRANSFAC | yes | 71052621 | ||
chr3 | 130841368 | 130841378 | MAX | JASPAR | yes | 71052622 | ||
chr3 | 130841368 | 130841379 | USF1 | JASPAR | yes | 71052623 | ||
chr3 | 130841368 | 130841379 | USF2 | JASPAR | yes | 71052624 | ||
chr3 | 130841369 | 130841379 | NEUROD2 | JASPAR | yes | 71052625 | ||
chr3 | 130841372 | 130841387 | HNF4G | JASPAR | yes | 71052626 | ||
chr3 | 130841373 | 130841388 | HNF4A | JASPAR | yes | 71052627 | ||
chr3 | 130841388 | 130841391 | MYB | TRANSFAC | yes | 71052628 | ||
chr3 | 130841415 | 130841421 | SOX10 | JASPAR | yes | 71052629 | ||
chr3 | 130841444 | 130841453 | NFIX | JASPAR | yes | 71052630 | ||
chr3 | 130841445 | 130841451 | NFIC | JASPAR | yes | 71052631 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
chr3 | 130732719 | 130746493 | - | ASTE1 | ENSG00000034533.7 | 130746493 | 0.73 | 0.99 | 4081 | 5129 | |
chr3 | 130745694 | 131069309 | + | NEK11 | ENSG00000114670.9 | 130745694 | 0.81 | 0.98 | 4082 | 4330 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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