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 |
|---|---|---|---|---|---|---|---|---|
| chr16 | 70356792 | 70356807 | FOXP1 | JASPAR | yes | 49388635 | ||
| chr16 | 70356793 | 70356808 | FOXP1 | JASPAR | yes | 49388636 | ||
| chr16 | 70356794 | 70356809 | FOXP1 | JASPAR | yes | 49388637 | ||
| chr16 | 70356795 | 70356810 | FOXP1 | JASPAR | yes | 49388638 | ||
| chr16 | 70356796 | 70356811 | FOXP1 | JASPAR | yes | 49388639 | ||
| chr16 | 70356797 | 70356812 | FOXP1 | JASPAR | yes | 49388640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16 | 70258261 | 70258641 | + | FKSG63 | ENSG00000269866.1 | 70258261 | 0.9 | 1.0 | 15019 | 1469 | |
| chr16 | 70284134 | 70285833 | - | EXOSC6 | ENSG00000223496.1 | 70285833 | 0.49 | 0.99 | 15020 | 29041 | |
| chr16 | 70286198 | 70323446 | - | AARS | ENSG00000090861.11 | 70323446 | 0.6 | 1.0 | 15021 | 66654 | |
| chr16 | 70323566 | 70369186 | + | DDX19B | ENSG00000157349.11 | 70323566 | 0.68 | 0.99 | 15022 | 66774 | |
| chr16 | 70333097 | 70400163 | + | RP11-529K1.3 | ENSG00000260537.1 | 70333097 | 0.92 | 0.87 | 15023 | 76305 | |
| chr16 | 70380732 | 70407286 | + | DDX19A | ENSG00000168872.11 | 70380732 | 0.56 | 0.99 | 15024 | 76080 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|