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 |
|---|---|---|---|---|---|---|---|---|
| chr19 | 52996443 | 52996658 | RAD21 | UCSC Txn Factor | no | Conserved | 108427055 | |
| chr19 | 52996637 | 52996641 | LFA1 | TRANSFAC | yes | 70875090 | ||
| chr19 | 52996642 | 52996646 | H4TF2 | TRANSFAC | yes | 70875091 | ||
| chr19 | 52996644 | 52996655 | EBF1 | JASPAR | yes | 70875092 | ||
| chr19 | 52996654 | 52996669 | HNF4A | JASPAR | yes | 70875093 | ||
| chr19 | 52996655 | 52996669 | RXRB | JASPAR | yes | 70875094 | ||
| chr19 | 52996655 | 52996669 | RXRG | JASPAR | yes | 70875095 | ||
| chr19 | 52996655 | 52996670 | HNF4G | JASPAR | yes | 70875096 | ||
| chr19 | 52996669 | 52996674 | GATA2 | JASPAR | yes | 70875097 | ||
| chr19 | 52996699 | 52996705 | ETS1 | JASPAR | yes | 70875098 | ||
| chr19 | 52996722 | 52996734 | PROX1 | JASPAR | yes | 70875099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19 | 52901102 | 52921665 | + | ZNF528 | ENSG00000167555.9 | 52901102 | 0.82 | 0.81 | 17952 | 4486 | |
| chr19 | 52932440 | 52955568 | + | ZNF534 | ENSG00000198633.6 | 52932440 | 0.79 | 0.99 | 17953 | 35824 | |
| chr19 | 52956829 | 53015407 | + | ZNF578 | ENSG00000258405.5 | 52956829 | 0.82 | 0.88 | 17954 | 60213 | |
| chr19 | 53030905 | 53067717 | + | ZNF808 | ENSG00000198482.6 | 53030905 | 0.81 | 0.99 | 17955 | 65829 | |
| chr19 | 53059075 | 53090427 | + | ZNF701 | ENSG00000167562.7 | 53059075 | 0.72 | 0.99 | 17956 | 37659 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|