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 | 74918685 | 74918700 | FOXP1 | JASPAR | yes | 107581207 | ||
| chr14 | 74918686 | 74918692 | TBP | TRANSFAC | yes | 107581208 | ||
| chr14 | 74918686 | 74918701 | FOXP1 | JASPAR | yes | 107581209 | ||
| chr14 | 74918686 | 74918707 | IRF1 | JASPAR | yes | 107581210 | ||
| chr14 | 74918687 | 74918702 | FOXP1 | JASPAR | yes | 107581211 | ||
| chr14 | 74918688 | 74918703 | FOXP1 | JASPAR | yes | 107581212 | ||
| chr14 | 74918689 | 74918704 | FOXP1 | JASPAR | yes | 107581213 | ||
| chr14 | 74918690 | 74918705 | FOXP1 | JASPAR | yes | 107581214 | ||
| chr14 | 74918691 | 74918706 | FOXP1 | JASPAR | yes | 107581215 | ||
| chr14 | 74918692 | 74918707 | FOXP1 | JASPAR | yes | 107581216 |
| 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 | 74872596 | 74892805 | - | SYNDIG1L | ENSG00000183379.4 | 74892805 | 0.91 | 1.0 | 13477 | 74121 | |
| chr14 | 74942895 | 74960880 | - | NPC2 | ENSG00000119655.4 | 74960880 | 0.84 | 0.99 | 13478 | 57827 | |
| chr14 | 74960423 | 74963809 | + | ISCA2 | ENSG00000165898.9 | 74960423 | 0.86 | 0.99 | 13479 | 58284 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14 | 74946838 | 74946860 | - | hsa-miR-4709-3p | MIMAT0019812 | 74960007 | 0.18842414130372245 | 0.916667 | 0.0 | 414 |