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 | 46701673 | 46705042 | EZH2 | UCSC Txn Factor | no | Conserved | 108268456 | |
| chr17 | 46702133 | 46704505 | POLR2A | UCSC Txn Factor | no | Conserved | 108268459 | |
| chr17 | 46702584 | 46702597 | SCRT2 | JASPAR | yes | 21251031 | ||
| chr17 | 46702599 | 46702609 | HOXB13 | JASPAR | yes | 21251032 | ||
| chr17 | 46702604 | 46702618 | POU1F1 | JASPAR | yes | 21251033 | ||
| chr17 | 46702608 | 46702629 | ZNF263 | JASPAR | yes | 21251034 | ||
| chr17 | 46702609 | 46702619 | EMX1 | JASPAR | yes | 21251035 | ||
| chr17 | 46702609 | 46702619 | EVX1 | JASPAR | yes | 21251036 | ||
| chr17 | 46702609 | 46702619 | EVX2 | JASPAR | yes | 21251037 | ||
| chr17 | 46702609 | 46702619 | NOTO | JASPAR | yes | 21251038 | ||
| chr17 | 46702610 | 46702620 | POU6F2 | JASPAR | yes | 21251039 | ||
| chr17 | 46702616 | 46702627 | E2F6 | JASPAR | yes | 21251040 | ||
| chr17 | 46702619 | 46702629 | SP1 | JASPAR | yes | 21251041 | ||
| chr17 | 46702622 | 46702632 | MZF1 | JASPAR | yes | 21251042 | ||
| chr17 | 46702622 | 46702634 | INSM1 | JASPAR | yes | 21251043 | ||
| chr17 | 46702623 | 46702638 | NR2C2 | JASPAR | yes | 21251044 | ||
| chr17 | 46702625 | 46702635 | SP1 | JASPAR | yes | 21251045 | ||
| chr17 | 46702684 | 46702699 | TFAP2C | JASPAR | yes | 21251046 | ||
| chr17 | 46702686 | 46702698 | TFAP2A | JASPAR | yes | 21251047 | ||
| chr17 | 46702686 | 46702698 | TFAP2B | JASPAR | yes | 21251048 | ||
| chr17 | 46702686 | 46702698 | TFAP2C | JASPAR | yes | 21251049 | ||
| chr17 | 46702688 | 46702697 | TFAP2A | JASPAR | yes | 21251050 | ||
| chr17 | 46702693 | 46702697 | LFA1 | TRANSFAC | yes | 21251051 | ||
| chr17 | 46702710 | 46702725 | HNF4A | JASPAR | yes | 21251052 | ||
| chr17 | 46702711 | 46702726 | HNF4G | JASPAR | yes | 21251053 | ||
| chr17 | 46702711 | 46702726 | NR2C2 | JASPAR | yes | 21251054 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 46702628 | rs115739674 | C | G,T |
|
4911204 | |
| chr17 | 46702634 | rs78306280 | C | T |
|
4911205 | |
| chr17 | 46702643 | rs2875820 | G | A |
|
4911206 | |
| chr17 | 46702683 | rs35566795 | C | T |
|
4911207 |
| 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 | 46605888 | 46608359 | - | HOXB1 | ENSG00000120094.6 | 46608359 | 0.98 | 1.0 | 15990 | 5780 | |
| chr17 | 46618256 | 46623441 | - | HOXB2 | ENSG00000173917.9 | 46623441 | 0.8 | 0.98 | 15991 | 20862 | |
| chr17 | 46626232 | 46682274 | - | HOXB3 | ENSG00000120093.7 | 46682274 | 0.96 | 1.0 | 15992 | 79695 | |
| chr17 | 46652875 | 46657473 | - | HOXB4 | ENSG00000182742.5 | 46657473 | 0.87 | 0.99 | 15993 | 54894 | |
| chr17 | 46668619 | 46671323 | - | HOXB5 | ENSG00000120075.5 | 46671323 | 0.95 | 1.0 | 15994 | 68744 | |
| chr17 | 46671639 | 46682354 | - | HOXB6 | ENSG00000108511.8 | 46682354 | 0.99 | 1.0 | 15995 | 79775 | |
| chr17 | 46684594 | 46710934 | - | HOXB7 | ENSG00000260027.3 | 46710934 | 0.95 | 1.0 | 15996 | 91815 | |
| chr17 | 46688739 | 46692478 | - | HOXB8 | ENSG00000120068.5 | 46692478 | 0.99 | 1.0 | 15997 | 89899 | |
| chr17 | 46698518 | 46703839 | - | HOXB9 | ENSG00000170689.8 | 46703839 | 0.99 | 1.0 | 15998 | 98910 | |
| chr17 | 46799084 | 46799884 | - | PRAC1 | ENSG00000159182.3 | 46799884 | 1.0 | 1.0 | 15999 | 2865 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|