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 |
|---|---|---|---|---|---|---|---|---|
| chr1 | 6451771 | 6451789 | ESR2 | JASPAR | yes | 118221673 | ||
| chr1 | 6451772 | 6451789 | ESR1 | JASPAR | yes | 118221674 | ||
| chr1 | 6451772 | 6451790 | ESR2 | JASPAR | yes | 118221675 | ||
| chr1 | 6451773 | 6451788 | ESR2 | JASPAR | yes | 118221676 | ||
| chr1 | 6451773 | 6451793 | ESR1 | JASPAR | yes | 118221677 | ||
| chr1 | 6451815 | 6451826 | FLI1 | JASPAR | yes | 118221678 | ||
| chr1 | 6451816 | 6451820 | YY1 | TRANSFAC | yes | 118221679 | ||
| chr1 | 6451816 | 6451829 | ELF1 | JASPAR | yes | 118221680 | ||
| chr1 | 6451817 | 6451825 | FEV | JASPAR | yes | 118221681 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr1 | 6451783 | rs186888136 | T | C |
|
38933 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1 | 6324329 | 6454451 | - | ACOT7 | ENSG00000097021.15 | 6454451 | 0.94 | 1.0 | 96 | 97380 | |
| chr1 | 6472478 | 6484730 | - | HES2 | ENSG00000069812.7 | 6484730 | 0.96 | 1.0 | 97 | 67101 | |
| chr1 | 6484848 | 6521430 | + | ESPN | ENSG00000187017.10 | 6484848 | 0.94 | 1.0 | 98 | 66983 | |
| chr1 | 6521211 | 6526255 | - | TNFRSF25 | ENSG00000215788.5 | 6526255 | 0.87 | 1.0 | 99 | 25576 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|