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 |
|---|---|---|---|---|---|---|---|---|
| chr11 | 1805021 | 1805031 | SP1 | JASPAR | yes | 36969424 | ||
| chr11 | 1805021 | 1805031 | SP1 | JASPAR | yes | 114028710 | ||
| chr11 | 1805021 | 1805042 | ZNF263 | JASPAR | yes | 36969425 | ||
| chr11 | 1805021 | 1805042 | ZNF263 | JASPAR | yes | 114028711 | ||
| chr11 | 1805026 | 1805041 | PRDM1 | JASPAR | yes | 36969426 | ||
| chr11 | 1805026 | 1805041 | PRDM1 | JASPAR | yes | 114028712 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr11 | 1805022 | rs35000338 | G | C |
|
1796450 | |
| chr11 | 1805027 | rs74469078 | A | T |
|
1796451 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11 | 1718425 | 1718985 | + | KRTAP5-6 | ENSG00000205864.1 | 1718425 | 0.99 | 0.0 | 10398 | 13424 | |
| chr11 | 1753640 | 1771821 | - | IFITM10 | ENSG00000244242.1 | 1771821 | 0.94 | 0.97 | 10399 | 66820 | |
| chr11 | 1768897 | 1780281 | - | RP11-295K3.1 | ENSG00000250644.1 | 1780281 | 0.95 | 0.8 | 10400 | 75280 | |
| chr11 | 1773982 | 1785222 | - | CTSD | ENSG00000117984.8 | 1785222 | 0.74 | 0.98 | 10401 | 80221 | |
| chr11 | 1848709 | 1858751 | + | SYT8 | ENSG00000149043.12 | 1848709 | 0.93 | 1.0 | 10402 | 56339 | |
| chr11 | 1860219 | 1862910 | + | TNNI2 | ENSG00000130598.11 | 1860219 | 0.86 | 0.96 | 10403 | 44829 | |
| chr11 | 1874200 | 1913497 | + | LSP1 | ENSG00000130592.9 | 1874200 | 0.9 | 0.9 | 10404 | 30848 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|