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 |
|---|---|---|---|---|---|---|---|---|
| chr17 | 10828054 | 10828059 | ETS2 | TRANSFAC | yes | 21199837 | ||
| chr17 | 10828061 | 10828065 | NFE | TRANSFAC | yes | 21199838 | ||
| chr17 | 10828065 | 10828075 | SREBF1 | JASPAR | yes | 21199839 | ||
| chr17 | 10828065 | 10828075 | SREBF2 | JASPAR | yes | 21199840 | ||
| chr17 | 10828068 | 10828089 | ZNF263 | JASPAR | yes | 21199841 | ||
| chr17 | 10828079 | 10828089 | SP1 | JASPAR | yes | 21199842 | ||
| chr17 | 10828080 | 10828087 | CEBPA | TRANSFAC | yes | 21199843 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 10725792 | 10741762 | - | PIRT | ENSG00000233670.6 | 10741762 | 0.98 | 1.0 | 15448 | 13712 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|