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 | 78229808 | 78229823 | JUND | JASPAR | yes | 21314265 | ||
| chr17 | 78229809 | 78229822 | JUN | JASPAR | yes | 21314266 | ||
| chr17 | 78229832 | 78229837 | SP1 | TRANSFAC | yes | 21314267 | ||
| chr17 | 78229838 | 78229847 | PITX3 | JASPAR | yes | 21314268 | ||
| chr17 | 78229838 | 78229848 | GSC2 | JASPAR | yes | 21314269 | ||
| chr17 | 78229838 | 78229848 | GSC | JASPAR | yes | 21314270 | ||
| chr17 | 78229839 | 78229847 | OTX2 | JASPAR | yes | 21314271 | ||
| chr17 | 78229848 | 78229852 | TEAD2 | TRANSFAC | yes | 21314272 | ||
| chr17 | 78229858 | 78229872 | SPI1 | JASPAR | yes | 21314273 | ||
| chr17 | 78229862 | 78229877 | FOXP1 | JASPAR | yes | 21314274 | ||
| chr17 | 78229869 | 78229875 | TCF4 | TRANSFAC | yes | 21314275 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 78143791 | 78183130 | + | CARD14 | ENSG00000141527.12 | 78143791 | 0.85 | 1.0 | 16333 | 13984 | |
| chr17 | 78180515 | 78194722 | - | SGSH | ENSG00000181523.8 | 78194722 | 0.66 | 1.0 | 16334 | 64915 | |
| chr17 | 78193498 | 78227299 | + | SLC26A11 | ENSG00000181045.10 | 78193498 | 0.72 | 1.0 | 16335 | 63691 | |
| chr17 | 78234665 | 78372586 | + | RNF213 | ENSG00000173821.15 | 78234665 | 0.88 | 1.0 | 16336 | 95214 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|