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 |
|---|---|---|---|---|---|---|---|---|
| chr9 | 35153448 | 35153463 | FOXP1 | JASPAR | yes | 95347821 | ||
| chr9 | 35153449 | 35153464 | FOXP1 | JASPAR | yes | 95347822 | ||
| chr9 | 35153450 | 35153465 | FOXP1 | JASPAR | yes | 95347823 | ||
| chr9 | 35153451 | 35153466 | FOXP1 | JASPAR | yes | 95347824 | ||
| chr9 | 35153452 | 35153467 | FOXP1 | JASPAR | yes | 95347825 | ||
| chr9 | 35153453 | 35153468 | FOXP1 | JASPAR | yes | 95347826 | ||
| chr9 | 35153454 | 35153469 | FOXP1 | JASPAR | yes | 95347827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9 | 35056061 | 35073246 | - | VCP | ENSG00000165280.11 | 35073246 | 0.59 | 1.0 | 8919 | 19798 | |
| chr9 | 35073832 | 35080013 | - | FANCG | ENSG00000221829.5 | 35080013 | 0.81 | 1.0 | 8920 | 26565 | |
| chr9 | 35088685 | 35096591 | - | PIGO | ENSG00000165282.9 | 35096591 | 0.69 | 1.0 | 8921 | 43143 | |
| chr9 | 35099888 | 35103154 | - | STOML2 | ENSG00000165283.11 | 35103154 | 0.69 | 1.0 | 8922 | 49706 | |
| chr9 | 35104109 | 35116338 | - | FAM214B | ENSG00000005238.15 | 35116338 | 0.73 | 1.0 | 8923 | 62890 | |
| chr9 | 35161999 | 35405335 | + | UNC13B | ENSG00000198722.8 | 35161999 | 0.86 | 1.0 | 8924 | 91470 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|