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 | 3831159 | 3831180 | ZNF263 | JASPAR | yes | 114033174 | ||
| chr11 | 3831162 | 3831167 | SP1 | TRANSFAC | yes | 114033175 | ||
| chr11 | 3831169 | 3831184 | PRDM1 | JASPAR | yes | 114033176 | ||
| chr11 | 3831176 | 3831196 | RREB1 | JASPAR | yes | 114033177 | ||
| chr11 | 3831178 | 3831193 | RUNX2 | JASPAR | yes | 114033178 | ||
| chr11 | 3831185 | 3831195 | SP1 | JASPAR | yes | 114033179 | ||
| chr11 | 3831186 | 3831196 | SP1 | JASPAR | yes | 114033180 | ||
| chr11 | 3831188 | 3831193 | SP1 | TRANSFAC | yes | 114033181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11 | 3692313 | 3819022 | - | NUP98 | ENSG00000110713.11 | 3819022 | 0.64 | 1.0 | 10433 | 87876 | |
| chr11 | 3818954 | 3847601 | + | PGAP2 | ENSG00000148985.15 | 3818954 | 0.67 | 1.0 | 10434 | 87808 | |
| chr11 | 3848208 | 3862213 | - | RHOG | ENSG00000177105.9 | 3862213 | 0.83 | 1.0 | 10435 | 68984 | |
| chr11 | 3875757 | 4114439 | + | STIM1 | ENSG00000167323.5 | 3875757 | 0.66 | 1.0 | 10436 | 55440 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11 | 3877343 | 3877363 | + | hsa-miR-4687-3p | MIMAT0019775 | 3876893 | 0.19123547496222187 | 0.858202 | 0.0 | 205 |