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 |
|---|---|---|---|---|---|---|---|---|
| chr11 | 125697407 | 125697415 | CREB1 | JASPAR | yes | 114151263 | ||
| chr11 | 125697437 | 125697452 | RUNX2 | JASPAR | yes | 114151264 | ||
| chr11 | 125697438 | 125697447 | RUNX2 | JASPAR | yes | 114151265 | ||
| chr11 | 125697438 | 125697448 | RUNX3 | JASPAR | yes | 114151266 | ||
| chr11 | 125697438 | 125697449 | RUNX1 | JASPAR | yes | 114151267 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr11 | 125697442 | rs75177485 | C | A |
|
2342217 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11 | 125616188 | 125619762 | + | PATE1 | ENSG00000171053.5 | 125616188 | 1.0 | 0.95 | 11608 | 18781 | |
| chr11 | 125646008 | 125648714 | - | PATE2 | ENSG00000196844.4 | 125648714 | 0.85 | 0.95 | 11609 | 51307 | |
| chr11 | 125658006 | 125661495 | + | PATE3 | ENSG00000236027.2 | 125658006 | 0.0 | 0.93 | 11610 | 60599 | |
| chr11 | 125703211 | 125709964 | + | PATE4 | ENSG00000237353.2 | 125703211 | 0.97 | 0.86 | 11611 | 94251 | |
| chr11 | 125753509 | 125770543 | + | HYLS1 | ENSG00000198331.6 | 125753509 | 0.8 | 0.99 | 11612 | 43953 | |
| chr11 | 125763381 | 125773116 | - | PUS3 | ENSG00000110060.4 | 125773116 | 0.72 | 0.99 | 11613 | 24346 | |
| chr11 | 125773271 | 125793158 | + | DDX25 | ENSG00000109832.8 | 125773271 | 0.92 | 1.0 | 11614 | 24191 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|