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 |
|---|---|---|---|---|---|---|---|---|
| chr2 | 216135072 | 216135087 | HNF4G | JASPAR | yes | 22203504 | ||
| chr2 | 216135072 | 216135087 | HNF4G | JASPAR | yes | 80760422 | ||
| chr2 | 216135080 | 216135091 | STAT1 | JASPAR | yes | 22203505 | ||
| chr2 | 216135080 | 216135091 | STAT3 | JASPAR | yes | 22203506 | ||
| chr2 | 216135080 | 216135091 | STAT1 | JASPAR | yes | 80760423 | ||
| chr2 | 216135080 | 216135091 | STAT3 | JASPAR | yes | 80760424 | ||
| chr2 | 216135085 | 216135100 | FOXP1 | JASPAR | yes | 22203507 | ||
| chr2 | 216135085 | 216135100 | FOXP1 | JASPAR | yes | 80760425 | ||
| chr2 | 216135086 | 216135101 | FOXP1 | JASPAR | yes | 22203508 | ||
| chr2 | 216135086 | 216135101 | FOXP1 | JASPAR | yes | 80760426 | ||
| chr2 | 216135087 | 216135102 | FOXP1 | JASPAR | yes | 22203509 | ||
| chr2 | 216135087 | 216135102 | FOXP1 | JASPAR | yes | 80760427 | ||
| chr2 | 216135088 | 216135103 | FOXP1 | JASPAR | yes | 22203510 | ||
| chr2 | 216135088 | 216135103 | FOXP1 | JASPAR | yes | 80760428 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr2 | 216135087 | rs573796764 | A | G |
|
6344475 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2 | 216176540 | 216214487 | + | ATIC | ENSG00000138363.10 | 216176540 | 0.87 | 0.99 | 3116 | 58554 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|