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 | 9769945 | 9770614 | CTCF | UCSC Txn Factor | no | Conserved | 107956334 | |
| chr11 | 9770019 | 9770362 | SMC3 | UCSC Txn Factor | no | Conserved | 107956349 | |
| chr11 | 9770076 | 9770328 | RAD21 | UCSC Txn Factor | no | Conserved | 107956360 | |
| chr11 | 9770045 | 9770066 | MAFG | JASPAR | yes | 114038627 | ||
| chr11 | 9770063 | 9770080 | RARA | JASPAR | yes | 114038628 | ||
| chr11 | 9770064 | 9770079 | ZIC3 | JASPAR | yes | 114038629 | ||
| chr11 | 9770064 | 9770079 | ZIC4 | JASPAR | yes | 114038630 | ||
| chr11 | 9770065 | 9770079 | GLIS3 | JASPAR | yes | 114038631 | ||
| chr11 | 9770090 | 9770099 | THAP1 | JASPAR | yes | 114038632 | ||
| chr11 | 9770091 | 9770103 | TFAP2C | JASPAR | yes | 114038633 | ||
| chr11 | 9770091 | 9770106 | TFAP2A | JASPAR | yes | 114038634 | ||
| chr11 | 9770091 | 9770110 | CTCF | JASPAR | yes | 114038635 | ||
| chr11 | 9770126 | 9770142 | ZNF143 | JASPAR | yes | 114038636 | ||
| chr11 | 9770130 | 9770145 | ZIC3 | JASPAR | yes | 114038637 | ||
| chr11 | 9770130 | 9770145 | ZIC4 | JASPAR | yes | 114038638 | ||
| chr11 | 9770131 | 9770145 | ZIC1 | JASPAR | yes | 114038639 | ||
| chr11 | 9770148 | 9770161 | SCRT2 | JASPAR | yes | 114038640 | ||
| chr11 | 9770179 | 9770190 | NFKB1 | JASPAR | yes | 114038641 | ||
| chr11 | 9770180 | 9770190 | NFKB1 | JASPAR | yes | 114038642 | ||
| chr11 | 9770180 | 9770190 | REL | JASPAR | yes | 114038643 | ||
| chr11 | 9770187 | 9770198 | E2F6 | JASPAR | yes | 114038644 | ||
| chr11 | 9770187 | 9770208 | ZNF263 | JASPAR | yes | 114038645 | ||
| chr11 | 9770188 | 9770209 | ZNF263 | JASPAR | yes | 114038646 | ||
| chr11 | 9770208 | 9770227 | CTCF | JASPAR | yes | 114038647 | ||
| chr11 | 9770223 | 9770229 | SOX10 | JASPAR | yes | 114038648 | ||
| chr11 | 9770257 | 9770261 | YY1 | TRANSFAC | yes | 114038649 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr11 | 9770093 | rs145122552 | G | C |
|
1836438 | |
| chr11 | 9770128 | rs188954138 | T | C |
|
1836439 | |
| chr11 | 9770186 | rs557537477 | GTCCC | G |
|
1836440 | |
| chr11 | 9770250 | rs34552339 | A | AG |
|
1836441 | |
| chr11 | 9770250 | rs397740484 | A | AG |
|
1836442 |
| 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 | 9685624 | 9774538 | + | SWAP70 | ENSG00000133789.10 | 9685624 | 0.7 | 0.99 | 10569 | 15596 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|