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 |
|---|---|---|---|---|---|---|---|---|
| chr14 | 99763125 | 99763134 | NKX2-8 | JASPAR | yes | 107609217 | ||
| chr14 | 99763139 | 99763155 | SOX4 | JASPAR | yes | 107609218 | ||
| chr14 | 99763140 | 99763155 | SOX21 | JASPAR | yes | 107609219 | ||
| chr14 | 99763150 | 99763164 | JUN | JASPAR | yes | 107609220 | ||
| chr14 | 99763152 | 99763163 | BATF | JASPAR | yes | 107609221 | ||
| chr14 | 99763154 | 99763165 | FOS | JASPAR | yes | 107609222 | ||
| chr14 | 99763154 | 99763165 | FOSL1 | JASPAR | yes | 107609223 | ||
| chr14 | 99763155 | 99763164 | JDP2 | JASPAR | yes | 107609224 | ||
| chr14 | 99763167 | 99763173 | MZF1 | JASPAR | yes | 107609225 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr14 | 99763139 | rs72702676 | G | A |
|
3781017 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14 | 99635624 | 99737861 | - | BCL11B | ENSG00000127152.13 | 99737861 | 0.95 | 0.99 | 13628 | 74770 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|