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 | 62089105 | 62089126 | IRF1 | JASPAR | yes | 107562254 | ||
| chr14 | 62089105 | 62089126 | IRF1 | JASPAR | yes | 115870279 | ||
| chr14 | 62089107 | 62089122 | STAT2 | JASPAR | yes | 107562255 | ||
| chr14 | 62089107 | 62089122 | STAT2 | JASPAR | yes | 115870280 | ||
| chr14 | 62089121 | 62089124 | MYB | TRANSFAC | yes | 107562256 | ||
| chr14 | 62089121 | 62089124 | MYB | TRANSFAC | yes | 115870281 | ||
| chr14 | 62089124 | 62089128 | NFE | TRANSFAC | yes | 107562257 | ||
| chr14 | 62089124 | 62089128 | NFE | TRANSFAC | yes | 115870282 | ||
| chr14 | 62089124 | 62089139 | FOXP1 | JASPAR | yes | 107562258 | ||
| chr14 | 62089124 | 62089139 | FOXP1 | JASPAR | yes | 115870283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14 | 61995846 | 62124682 | + | RP11-47I22.4 | ENSG00000258989.1 | 61995846 | 0.93 | 0.77 | 13379 | 6731 | |
| chr14 | 62037258 | 62125414 | + | RP11-47I22.3 | ENSG00000232774.3 | 62037258 | 0.87 | 0.99 | 13380 | 48143 | |
| chr14 | 62162231 | 62214976 | + | HIF1A | ENSG00000100644.12 | 62162231 | 0.77 | 0.98 | 13381 | 26893 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|