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 |
|---|---|---|---|---|---|---|---|---|
| chr1 | 55445620 | 55445631 | NRF1 | JASPAR | yes | 118293944 | ||
| chr1 | 55445633 | 55445636 | MYB | TRANSFAC | yes | 118293945 | ||
| chr1 | 55445636 | 55445646 | SP1 | JASPAR | yes | 118293946 | ||
| chr1 | 55445637 | 55445645 | EHF | JASPAR | yes | 118293947 | ||
| chr1 | 55445637 | 55445652 | TFAP2C | JASPAR | yes | 118293948 | ||
| chr1 | 55445656 | 55445666 | FIGLA | JASPAR | yes | 118293949 | ||
| chr1 | 55445656 | 55445666 | SREBF2 | JASPAR | yes | 118293950 | ||
| chr1 | 55445658 | 55445663 | USF2 | TRANSFAC | yes | 118293951 | ||
| chr1 | 55445661 | 55445665 | NFE | TRANSFAC | yes | 118293952 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr1 | 55445613 | rs2433674 | A | G | no | 324006 | |
| chr1 | 55445628 | rs536318821 | C | T |
|
324007 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1 | 55315306 | 55352891 | - | DHCR24 | ENSG00000116133.7 | 55352891 | 0.91 | 0.99 | 740 | 7299 | |
| chr1 | 55446465 | 55457966 | + | TMEM61 | ENSG00000143001.4 | 55446465 | 0.91 | 1.0 | 741 | 99218 | |
| chr1 | 55464606 | 55476556 | + | BSND | ENSG00000162399.6 | 55464606 | 1.0 | 0.98 | 742 | 81077 | |
| chr1 | 55505221 | 55530525 | + | PCSK9 | ENSG00000169174.9 | 55505221 | 0.96 | 1.0 | 743 | 40462 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|