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 | 109714119 | 109714122 | MYB | TRANSFAC | yes | 85996664 | ||
| chr9 | 109714119 | 109714122 | MYB | TRANSFAC | yes | 95392094 | ||
| chr9 | 109714126 | 109714147 | IRF1 | JASPAR | yes | 85996665 | ||
| chr9 | 109714126 | 109714147 | IRF1 | JASPAR | yes | 95392095 | ||
| chr9 | 109714127 | 109714142 | FOXP1 | JASPAR | yes | 85996666 | ||
| chr9 | 109714127 | 109714142 | FOXP1 | JASPAR | yes | 95392096 | ||
| chr9 | 109714127 | 109714148 | IRF1 | JASPAR | yes | 85996667 | ||
| chr9 | 109714127 | 109714148 | IRF1 | JASPAR | yes | 95392097 | ||
| chr9 | 109714128 | 109714139 | FOXP2 | JASPAR | yes | 85996668 | ||
| chr9 | 109714128 | 109714139 | FOXP2 | JASPAR | yes | 95392098 | ||
| chr9 | 109714128 | 109714143 | STAT2 | JASPAR | yes | 85996669 | ||
| chr9 | 109714128 | 109714143 | STAT2 | JASPAR | yes | 95392099 | ||
| chr9 | 109714129 | 109714144 | FOXP1 | JASPAR | yes | 85996670 | ||
| chr9 | 109714129 | 109714144 | FOXP1 | JASPAR | yes | 95392100 | ||
| chr9 | 109714131 | 109714146 | FOXP1 | JASPAR | yes | 85996671 | ||
| chr9 | 109714131 | 109714146 | FOXP1 | JASPAR | yes | 95392101 | ||
| chr9 | 109714132 | 109714147 | FOXP1 | JASPAR | yes | 85996672 | ||
| chr9 | 109714132 | 109714147 | FOXP1 | JASPAR | yes | 95392102 | ||
| chr9 | 109714133 | 109714148 | FOXP1 | JASPAR | yes | 85996673 | ||
| chr9 | 109714133 | 109714148 | FOXP1 | JASPAR | yes | 95392103 | ||
| chr9 | 109714134 | 109714149 | FOXP1 | JASPAR | yes | 85996674 | ||
| chr9 | 109714134 | 109714149 | FOXP1 | JASPAR | yes | 95392104 | ||
| chr9 | 109714142 | 109714152 | NFATC3 | JASPAR | yes | 85996675 | ||
| chr9 | 109714142 | 109714152 | NFATC3 | JASPAR | yes | 95392105 | ||
| chr9 | 109714143 | 109714150 | NFATC2 | JASPAR | yes | 85996676 | ||
| chr9 | 109714143 | 109714150 | NFATC2 | JASPAR | yes | 95392106 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr9 | 109714135 | rs181640166 | T | G |
|
11202136 |
| 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 | 109625378 | 109775915 | + | ZNF462 | ENSG00000148143.8 | 109625378 | 0.8 | 1.0 | 9200 | 11265 | |
| chr9 | 109685630 | 109686455 | + | RP11-508N12.4 | ENSG00000242631.2 | 109685630 | 0.98 | 1.0 | 9201 | 71517 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|