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 |
---|---|---|---|---|---|---|---|---|
chr17 | 1046730 | 1046741 | STAT3 | JASPAR | yes | 21180472 | ||
chr17 | 1046760 | 1046765 | SP1 | TRANSFAC | yes | 21180473 | ||
chr17 | 1046761 | 1046766 | SP1 | TRANSFAC | yes | 21180474 | ||
chr17 | 1046778 | 1046797 | RFX2 | JASPAR | yes | 21180475 | ||
chr17 | 1046780 | 1046795 | RFX5 | JASPAR | yes | 21180476 | ||
chr17 | 1046782 | 1046798 | RFX2 | JASPAR | yes | 21180477 | ||
chr17 | 1046782 | 1046798 | RFX3 | JASPAR | yes | 21180478 | ||
chr17 | 1046782 | 1046798 | RFX4 | JASPAR | yes | 21180479 | ||
chr17 | 1046782 | 1046798 | RFX5 | JASPAR | yes | 21180480 | ||
chr17 | 1046783 | 1046802 | RFX2 | JASPAR | yes | 21180481 | ||
chr17 | 1046797 | 1046810 | DUXA | JASPAR | yes | 21180482 | ||
chr17 | 1046798 | 1046809 | DUX4 | JASPAR | yes | 21180483 | ||
chr17 | 1046802 | 1046806 | H1TF2 | TRANSFAC | yes | 21180484 | ||
chr17 | 1046802 | 1046806 | NFE | TRANSFAC | yes | 21180485 | ||
chr17 | 1046802 | 1046806 | SRF | TRANSFAC | yes | 21180486 | ||
chr17 | 1046808 | 1046814 | ZNF354C | JASPAR | yes | 21180487 | ||
chr17 | 1046829 | 1046840 | E2F6 | JASPAR | yes | 21180488 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 1046738 | rs552493473 | G | C |
|
4690272 | |
chr17 | 1046747 | rs73975651 | C | G | no | 4690273 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr17 | 906758 | 1132315 | - | ABR | ENSG00000159842.10 | 1132315 | 0.65 | 1.0 | 15212 | 14526 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
---|