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 |
|---|---|---|---|---|---|---|---|---|
| chr3 | 124773900 | 124773905 | ETS2 | TRANSFAC | yes | 71043882 | ||
| chr3 | 124773903 | 124773909 | TCF4 | TRANSFAC | yes | 71043883 | ||
| chr3 | 124773905 | 124773919 | TCF7L2 | JASPAR | yes | 71043884 | ||
| chr3 | 124773932 | 124773938 | TCF4 | TRANSFAC | yes | 71043885 | ||
| chr3 | 124773955 | 124773961 | SOX10 | JASPAR | yes | 71043886 | ||
| chr3 | 124773970 | 124773975 | GATA2 | JASPAR | yes | 71043887 | ||
| chr3 | 124773986 | 124773996 | HOXA13 | JASPAR | yes | 71043888 | ||
| chr3 | 124773998 | 124774010 | FOXI1 | JASPAR | yes | 71043889 | ||
| chr3 | 124774001 | 124774005 | YY1 | TRANSFAC | yes | 71043890 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr3 | 124773896 | rs190544566 | C | A | no | 7001111 | |
| chr3 | 124773897 | rs2948801 | C | A | no | 7001112 | |
| chr3 | 124773949 | rs150939319 | G | A | no | 7001113 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3 | 124684554 | 124774802 | - | HEG1 | ENSG00000173706.8 | 124774802 | 0.83 | 0.96 | 4023 | 99218 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|