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 |
|---|---|---|---|---|---|---|---|---|
| chr17 | 53810086 | 53810101 | PRDM1 | JASPAR | yes | 21257689 | ||
| chr17 | 53810149 | 53810153 | YY1 | TRANSFAC | yes | 21257690 | ||
| chr17 | 53810152 | 53810156 | YY1 | TRANSFAC | yes | 21257691 | ||
| chr17 | 53810163 | 53810180 | PAX1 | JASPAR | yes | 21257692 | ||
| chr17 | 53810163 | 53810180 | PAX9 | JASPAR | yes | 21257693 | ||
| chr17 | 53810164 | 53810183 | PAX5 | JASPAR | yes | 21257694 | ||
| chr17 | 53810170 | 53810176 | LEF1 | TRANSFAC | yes | 21257695 | ||
| chr17 | 53810170 | 53810176 | SOX10 | JASPAR | yes | 21257696 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr17 | 53810080 | rs565599549 | A | C | no | 4941583 | |
| chr17 | 53810082 | rs577478948 | G | T | no | 4941584 | |
| chr17 | 53810178 | rs147934440 | G | T |
|
4941585 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 53796988 | 53809482 | - | TMEM100 | ENSG00000166292.7 | 53809482 | 0.97 | 0.93 | 16062 | 99415 | |
| chr17 | 53828340 | 53920191 | + | PCTP | ENSG00000141179.9 | 53828340 | 0.84 | 0.99 | 16063 | 81845 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|