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 |
|---|---|---|---|---|---|---|---|---|
| chr5 | 96476004 | 96476019 | LEF1 | JASPAR | yes | 70687789 | ||
| chr5 | 96476005 | 96476019 | TCF7L2 | JASPAR | yes | 70687790 | ||
| chr5 | 96476046 | 96476051 | ETS2 | TRANSFAC | yes | 70687791 | ||
| chr5 | 96476052 | 96476058 | NFIC | JASPAR | yes | 70687792 | ||
| chr5 | 96476066 | 96476075 | NKX2-8 | JASPAR | yes | 70687793 | ||
| chr5 | 96476066 | 96476076 | NKX2-3 | JASPAR | yes | 70687794 | ||
| chr5 | 96476083 | 96476088 | ETS2 | TRANSFAC | yes | 70687795 | ||
| chr5 | 96476105 | 96476126 | ZNF263 | JASPAR | yes | 70687796 | ||
| chr5 | 96476108 | 96476123 | NR2C2 | JASPAR | yes | 70687797 | ||
| chr5 | 96476120 | 96476130 | SP1 | JASPAR | yes | 70687798 | ||
| chr5 | 96476133 | 96476148 | RFX5 | JASPAR | yes | 70687799 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr5 | 96476104 | rs192162580 | T | C | no | 8395424 | |
| chr5 | 96476119 | rs138014623 | G | A |
|
8395425 | |
| chr5 | 96476135 | rs2544769 | C | G |
|
8395426 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5 | 96424779 | 96519354 | + | CTD-2215E18.1 | ENSG00000251606.1 | 96424779 | 0.96 | 1.0 | 5551 | 48789 | |
| chr5 | 96427574 | 96478576 | - | LIX1 | ENSG00000145721.7 | 96478576 | 0.96 | 0.96 | 5552 | 97594 | |
| chr5 | 96496571 | 96518964 | - | RIOK2 | ENSG00000058729.6 | 96518964 | 0.78 | 0.98 | 5553 | 57206 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|