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 |
|---|---|---|---|---|---|---|---|---|
| chr16 | 87490638 | 87490653 | HNF1A | JASPAR | yes | 12217522 | ||
| chr16 | 87490638 | 87490653 | HNF1A | JASPAR | yes | 49414152 | ||
| chr16 | 87490639 | 87490652 | HNF1B | JASPAR | yes | 12217523 | ||
| chr16 | 87490639 | 87490652 | HNF1B | JASPAR | yes | 49414153 | ||
| chr16 | 87490702 | 87490717 | NR2C2 | JASPAR | yes | 12217524 | ||
| chr16 | 87490702 | 87490717 | NR2C2 | JASPAR | yes | 49414154 | ||
| chr16 | 87490704 | 87490714 | SP1 | JASPAR | yes | 12217525 | ||
| chr16 | 87490704 | 87490714 | SP1 | JASPAR | yes | 49414155 | ||
| chr16 | 87490705 | 87490709 | LFA1 | TRANSFAC | yes | 12217526 | ||
| chr16 | 87490705 | 87490709 | LFA1 | TRANSFAC | yes | 49414156 | ||
| chr16 | 87490705 | 87490717 | INSM1 | JASPAR | yes | 12217527 | ||
| chr16 | 87490705 | 87490717 | INSM1 | JASPAR | yes | 49414157 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr16 | 87490667 | rs74853919 | G | A | no | 4650329 | |
| chr16 | 87490707 | rs375046824 | G | A |
|
4650330 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16 | 87360593 | 87425748 | - | FBXO31 | ENSG00000103264.11 | 87425748 | 0.64 | 1.0 | 15143 | 35127 | |
| chr16 | 87417601 | 87438385 | + | MAP1LC3B | ENSG00000140941.8 | 87417601 | 0.61 | 1.0 | 15144 | 26980 | |
| chr16 | 87439852 | 87525651 | - | ZCCHC14 | ENSG00000140948.7 | 87525651 | 0.7 | 1.0 | 15145 | 65068 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|