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 |
|---|---|---|---|---|---|---|---|---|
| chr19 | 19973353 | 19973365 | E2F8 | JASPAR | yes | 70825921 | ||
| chr19 | 19973356 | 19973376 | PPARG | JASPAR | yes | 70825922 | ||
| chr19 | 19973396 | 19973407 | HOXC13 | JASPAR | yes | 70825923 | ||
| chr19 | 19973413 | 19973430 | RXRA | JASPAR | yes | 70825924 | ||
| chr19 | 19973432 | 19973440 | FOXO3 | JASPAR | yes | 70825925 | ||
| chr19 | 19973459 | 19973462 | MYB | TRANSFAC | yes | 70825926 | ||
| chr19 | 19973460 | 19973470 | MYF6 | JASPAR | yes | 70825927 | ||
| chr19 | 19973468 | 19973479 | STAT3 | JASPAR | yes | 70825928 | ||
| chr19 | 19973482 | 19973486 | TEAD2 | TRANSFAC | yes | 70825929 | ||
| chr19 | 19973513 | 19973517 | H4TF2 | TRANSFAC | yes | 70825930 | ||
| chr19 | 19973521 | 19973531 | ETV3 | JASPAR | yes | 70825931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19 | 19896648 | 19932560 | - | ZNF506 | ENSG00000081665.9 | 19932560 | 0.71 | 0.97 | 17296 | 59233 | |
| chr19 | 19976695 | 20005483 | + | ZNF253 | ENSG00000256771.2 | 19976695 | 0.82 | 0.82 | 17297 | 96852 | |
| chr19 | 20011722 | 20046384 | + | ZNF93 | ENSG00000184635.9 | 20011722 | 0.83 | 0.91 | 17298 | 61825 | |
| chr19 | 20047769 | 20048639 | - | AC007204.1 | ENSG00000268461.1 | 20048639 | 0.93 | 0.0 | 17299 | 24908 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|