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 | 26201701 | 26201711 | SP1 | JASPAR | yes | 118254257 | ||
| chr1 | 26201702 | 26201713 | E2F6 | JASPAR | yes | 118254258 | ||
| chr1 | 26201721 | 26201726 | SP1 | TRANSFAC | yes | 118254259 | ||
| chr1 | 26201722 | 26201734 | INSM1 | JASPAR | yes | 118254260 | ||
| chr1 | 26201742 | 26201753 | FLI1 | JASPAR | yes | 118254261 | ||
| chr1 | 26201744 | 26201752 | EHF | JASPAR | yes | 118254262 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr1 | 26201724 | rs544949772 | G | T |
|
176616 |
| 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 | 26126667 | 26144713 | + | SEPN1 | ENSG00000162430.12 | 26126667 | 0.64 | 1.0 | 347 | 24968 | |
| chr1 | 26137961 | 26150235 | + | RP1-317E23.6 | ENSG00000255054.3 | 26137961 | 0.91 | 0.99 | 348 | 36262 | |
| chr1 | 26145131 | 26159432 | + | MTFR1L | ENSG00000117640.13 | 26145131 | 0.69 | 1.0 | 349 | 43432 | |
| chr1 | 26145212 | 26147288 | - | AL020996.1 | ENSG00000223474.2 | 26147288 | 0.74 | 1.0 | 350 | 45589 | |
| chr1 | 26158414 | 26185903 | - | AUNIP | ENSG00000127423.6 | 26185903 | 0.86 | 0.99 | 351 | 84204 | |
| chr1 | 26187701 | 26197744 | - | PAQR7 | ENSG00000182749.5 | 26197744 | 0.83 | 1.0 | 352 | 96045 | |
| chr1 | 26210672 | 26233482 | - | STMN1 | ENSG00000117632.16 | 26233482 | 0.97 | 0.98 | 353 | 68275 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|