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 | 9995279 | 9995294 | MEF2C | JASPAR | yes | 21198700 | ||
chr17 | 9995279 | 9995294 | MEF2C | JASPAR | yes | 53086033 | ||
chr17 | 9995281 | 9995296 | FOXP1 | JASPAR | yes | 21198701 | ||
chr17 | 9995281 | 9995296 | FOXP1 | JASPAR | yes | 53086034 | ||
chr17 | 9995282 | 9995297 | FOXP1 | JASPAR | yes | 21198702 | ||
chr17 | 9995282 | 9995297 | FOXP1 | JASPAR | yes | 53086035 | ||
chr17 | 9995283 | 9995289 | TBP | TRANSFAC | yes | 21198703 | ||
chr17 | 9995283 | 9995289 | TBP | TRANSFAC | yes | 53086036 | ||
chr17 | 9995283 | 9995298 | FOXP1 | JASPAR | yes | 21198704 | ||
chr17 | 9995283 | 9995298 | FOXP1 | JASPAR | yes | 53086037 | ||
chr17 | 9995284 | 9995299 | FOXP1 | JASPAR | yes | 21198705 | ||
chr17 | 9995284 | 9995299 | FOXP1 | JASPAR | yes | 53086038 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 9995284 | rs11429483 | T | TA,TAA |
|
4747846 | |
chr17 | 9995284 | rs397752039 | T | TA |
|
4747847 |
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 | 10048831 | 10050277 | + | AC000003.2 | ENSG00000264194.1 | 10048831 | 0.98 | 1.0 | 15438 | 46459 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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