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 |
|---|---|---|---|---|---|---|---|---|
| chr7 | 2697261 | 2697275 | PLAG1 | JASPAR | yes | 26016122 | ||
| chr7 | 2697273 | 2697288 | PRDM1 | JASPAR | yes | 26016123 | ||
| chr7 | 2697296 | 2697309 | ZBTB18 | JASPAR | yes | 26016124 | ||
| chr7 | 2697313 | 2697322 | HIC2 | JASPAR | yes | 26016125 | ||
| chr7 | 2697316 | 2697320 | LFA1 | TRANSFAC | yes | 26016126 | ||
| chr7 | 2697317 | 2697327 | NKX2-3 | JASPAR | yes | 26016127 | ||
| chr7 | 2697318 | 2697327 | NKX2-8 | JASPAR | yes | 26016128 | ||
| chr7 | 2697331 | 2697341 | BHLHE40 | JASPAR | yes | 26016129 | ||
| chr7 | 2697333 | 2697338 | MYC | TRANSFAC | yes | 26016130 | ||
| chr7 | 2697333 | 2697338 | USF1 | TRANSFAC | yes | 26016131 | ||
| chr7 | 2697333 | 2697338 | USF2 | TRANSFAC | yes | 26016132 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr7 | 2697271 | rs142231378 | G | A |
|
9584649 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7 | 2598632 | 2654368 | + | IQCE | ENSG00000106012.13 | 2598632 | 0.73 | 1.0 | 7178 | 1371 | |
| chr7 | 2671585 | 2704436 | + | TTYH3 | ENSG00000136295.10 | 2671585 | 0.88 | 1.0 | 7179 | 74324 | |
| chr7 | 2719156 | 2815134 | + | AMZ1 | ENSG00000174945.9 | 2719156 | 0.82 | 0.95 | 7180 | 78189 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|