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 |
|---|---|---|---|---|---|---|---|---|
| chr9 | 36231551 | 36231565 | STAT1 | JASPAR | yes | 95349299 | ||
| chr9 | 36231568 | 36231582 | IRF7 | JASPAR | yes | 95349300 | ||
| chr9 | 36231569 | 36231584 | PRDM1 | JASPAR | yes | 95349301 | ||
| chr9 | 36231569 | 36231587 | IRF2 | JASPAR | yes | 95349302 | ||
| chr9 | 36231582 | 36231603 | ZNF263 | JASPAR | yes | 95349303 | ||
| chr9 | 36231583 | 36231604 | ZNF263 | JASPAR | yes | 95349304 | ||
| chr9 | 36231586 | 36231601 | FOXP1 | JASPAR | yes | 95349305 | ||
| chr9 | 36231593 | 36231598 | ETS2 | TRANSFAC | yes | 95349306 | ||
| chr9 | 36231630 | 36231646 | RFX4 | JASPAR | yes | 95349307 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr9 | 36231556 | rs546798106 | T | C |
|
11007131 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9 | 36136732 | 36163910 | + | GLIPR2 | ENSG00000122694.11 | 36136732 | 0.72 | 1.0 | 8949 | 5185 | |
| chr9 | 36169389 | 36171329 | + | CCIN | ENSG00000185972.4 | 36169389 | 0.88 | 0.99 | 8950 | 37842 | |
| chr9 | 36190853 | 36304778 | + | CLTA | ENSG00000122705.12 | 36190853 | 0.64 | 0.99 | 8951 | 59306 | |
| chr9 | 36214438 | 36277053 | - | GNE | ENSG00000159921.10 | 36277053 | 0.82 | 0.98 | 8952 | 54613 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|