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 | 47059268 | 47059272 | TEAD2 | TRANSFAC | yes | 70860368 | ||
| chr19 | 47059268 | 47059273 | TBP | TRANSFAC | yes | 70860369 | ||
| chr19 | 47059268 | 47059274 | TFIID | TRANSFAC | yes | 70860370 | ||
| chr19 | 47059270 | 47059276 | TBP | TRANSFAC | yes | 70860371 | ||
| chr19 | 47059293 | 47059307 | SPI1 | JASPAR | yes | 70860372 | ||
| chr19 | 47059297 | 47059304 | SPIB | JASPAR | yes | 70860373 | ||
| chr19 | 47059304 | 47059308 | YY1 | TRANSFAC | yes | 70860374 | ||
| chr19 | 47059316 | 47059328 | PKNOX1 | JASPAR | yes | 70860375 | ||
| chr19 | 47059316 | 47059328 | PKNOX2 | JASPAR | yes | 70860376 | ||
| chr19 | 47059316 | 47059328 | TGIF1 | JASPAR | yes | 70860377 | ||
| chr19 | 47059316 | 47059328 | TGIF2 | JASPAR | yes | 70860378 | ||
| chr19 | 47059317 | 47059327 | TFAP4 | JASPAR | yes | 70860379 | ||
| chr19 | 47059327 | 47059339 | PBX1 | JASPAR | yes | 70860380 | ||
| chr19 | 47059351 | 47059361 | MEF2A | JASPAR | yes | 70860381 | ||
| chr19 | 47059352 | 47059356 | YY1 | TRANSFAC | yes | 70860382 | ||
| chr19 | 47059357 | 47059375 | MAFF | JASPAR | yes | 70860383 | ||
| chr19 | 47059359 | 47059370 | NRL | JASPAR | yes | 70860384 | ||
| chr19 | 47059359 | 47059374 | MAFK | JASPAR | yes | 70860385 | ||
| chr19 | 47059362 | 47059373 | STAT3 | JASPAR | yes | 70860386 | ||
| chr19 | 47059377 | 47059388 | FOXA1 | JASPAR | yes | 70860387 | ||
| chr19 | 47059377 | 47059392 | FOXA1 | JASPAR | yes | 70860388 | ||
| chr19 | 47059378 | 47059388 | NFIA | JASPAR | yes | 70860389 | ||
| chr19 | 47059378 | 47059389 | FOXC1 | JASPAR | yes | 70860390 | ||
| chr19 | 47059378 | 47059390 | FOXC2 | JASPAR | yes | 70860391 | ||
| chr19 | 47059380 | 47059386 | NFIC | JASPAR | yes | 70860392 | ||
| chr19 | 47059411 | 47059419 | OTX2 | JASPAR | yes | 70860393 |
| 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 | 46969748 | 46974820 | - | PNMAL1 | ENSG00000182013.13 | 46974820 | 0.82 | 0.95 | 17732 | 15552 | |
| chr19 | 46984053 | 47104457 | - | PPP5D1 | ENSG00000230510.2 | 47104457 | 0.81 | 0.99 | 17733 | 54966 | |
| chr19 | 46990163 | 46999755 | - | PNMAL2 | ENSG00000204851.5 | 46999755 | 0.89 | 0.95 | 17734 | 40487 | |
| chr19 | 46997765 | 46999755 | + | AC011484.1 | ENSG00000204850.3 | 46997765 | 0.91 | 1.0 | 17735 | 38497 | |
| chr19 | 47050313 | 47104118 | - | AC011551.3 | ENSG00000268423.1 | 47104118 | 0.78 | 0.87 | 17736 | 55305 | |
| chr19 | 47104331 | 47114050 | + | CALM3 | ENSG00000160014.12 | 47104331 | 0.68 | 1.0 | 17737 | 55092 | |
| chr19 | 47123725 | 47128375 | - | PTGIR | ENSG00000160013.4 | 47128375 | 0.9 | 0.96 | 17738 | 31048 | |
| chr19 | 47137333 | 47137942 | - | GNG8 | ENSG00000167414.4 | 47137942 | 0.9 | 0.93 | 17739 | 21481 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|