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 | 47113139 | 47113771 | CTCF | UCSC Txn Factor | no | Conserved | 108268960 | |
| chr17 | 47113433 | 47113699 | RAD21 | UCSC Txn Factor | no | Conserved | 108268984 | |
| chr17 | 47113513 | 47113525 | YY1 | JASPAR | yes | 21251602 | ||
| chr17 | 47113540 | 47113546 | SOX10 | JASPAR | yes | 21251603 | ||
| chr17 | 47113558 | 47113577 | CTCF | JASPAR | yes | 21251604 |
| 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 | 47006678 | 47022479 | - | SNF8 | ENSG00000159210.5 | 47022479 | 0.8 | 1.0 | 16005 | 8969 | |
| chr17 | 47035916 | 47045958 | - | GIP | ENSG00000159224.4 | 47045958 | 0.97 | 0.97 | 16006 | 32448 | |
| chr17 | 47074774 | 47133012 | + | IGF2BP1 | ENSG00000159217.5 | 47074774 | 0.96 | 0.88 | 16007 | 61264 | |
| chr17 | 47209822 | 47247351 | + | B4GALNT2 | ENSG00000167080.4 | 47209822 | 0.95 | 0.85 | 16008 | 3758 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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