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 | 1015158 | 1015173 | RFX5 | JASPAR | yes | 114026710 | ||
| chr11 | 1015158 | 1015173 | TFAP2C | JASPAR | yes | 114026711 | ||
| chr11 | 1015159 | 1015163 | NFE | TRANSFAC | yes | 114026712 | ||
| chr11 | 1015162 | 1015168 | MZF1 | JASPAR | yes | 114026713 | ||
| chr11 | 1015216 | 1015221 | ETS2 | TRANSFAC | yes | 114026714 | ||
| chr11 | 1015240 | 1015246 | NFIC | JASPAR | yes | 114026715 | ||
| chr11 | 1015258 | 1015267 | SNAI2 | JASPAR | yes | 114026716 | ||
| chr11 | 1015258 | 1015268 | ID4 | JASPAR | yes | 114026717 | ||
| chr11 | 1015258 | 1015268 | TCF3 | JASPAR | yes | 114026718 | ||
| chr11 | 1015258 | 1015268 | TCF4 | JASPAR | yes | 114026719 | ||
| chr11 | 1015278 | 1015282 | H4TF2 | TRANSFAC | yes | 114026720 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr11 | 1015182 | rs115411304 | C | T | no | 1790535 | |
| chr11 | 1015199 | rs79655259 | C | T | no | 1790536 | |
| chr11 | 1015201 | rs35792686 | C | T | no | 1790537 | |
| chr11 | 1015217 | rs534345670 | G | A |
|
1790538 |
| 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 | 924894 | 1012239 | + | AP2A2 | ENSG00000183020.9 | 924894 | 0.75 | 1.0 | 10383 | 9755 | |
| chr11 | 1012821 | 1036706 | - | MUC6 | ENSG00000184956.11 | 1036706 | 0.98 | 1.0 | 10384 | 78591 | |
| chr11 | 1074875 | 1104419 | + | MUC2 | ENSG00000198788.7 | 1074875 | 1.0 | 1.0 | 10385 | 40422 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|