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 | 33447673 | 33447685 | HNF1B | JASPAR | yes | 28018923 | ||
| chr1 | 33447673 | 33447685 | HNF1B | JASPAR | yes | 118269148 | ||
| chr1 | 33447689 | 33447694 | ETS2 | TRANSFAC | yes | 28018924 | ||
| chr1 | 33447689 | 33447694 | ETS2 | TRANSFAC | yes | 118269149 | ||
| chr1 | 33447689 | 33447697 | EHF | JASPAR | yes | 28018925 | ||
| chr1 | 33447689 | 33447697 | EHF | JASPAR | yes | 118269150 | ||
| chr1 | 33447699 | 33447710 | STAT3 | JASPAR | yes | 28018926 | ||
| chr1 | 33447699 | 33447710 | STAT3 | JASPAR | yes | 118269151 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|
| 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 | 33351595 | 33364042 | + | HPCA | ENSG00000121905.5 | 33351595 | 0.81 | 1.0 | 469 | 3928 | |
| chr1 | 33360195 | 33367039 | - | TMEM54 | ENSG00000121900.14 | 33367039 | 0.81 | 1.0 | 470 | 19372 | |
| chr1 | 33402046 | 33430286 | - | RNF19B | ENSG00000116514.12 | 33430286 | 0.66 | 1.0 | 471 | 82619 | |
| chr1 | 33439268 | 33439642 | + | FKSG48 | ENSG00000267885.1 | 33439268 | 0.84 | 1.0 | 472 | 91601 | |
| chr1 | 33473585 | 33546597 | - | AK2 | ENSG00000004455.12 | 33546597 | 0.77 | 1.0 | 473 | 1110 | |
| chr1 | 33546705 | 33586131 | + | ADC | ENSG00000142920.12 | 33546705 | 0.69 | 1.0 | 474 | 1002 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|