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 |
|---|---|---|---|---|---|---|---|---|
| chr12 | 49762005 | 49762025 | TP53 | JASPAR | yes | 82400382 | ||
| chr12 | 49762005 | 49762025 | TP53 | JASPAR | yes | 120774228 | ||
| chr12 | 49762033 | 49762050 | NR3C1 | JASPAR | yes | 82400383 | ||
| chr12 | 49762033 | 49762050 | NR3C2 | JASPAR | yes | 82400384 | ||
| chr12 | 49762033 | 49762050 | NR3C1 | JASPAR | yes | 120774229 | ||
| chr12 | 49762033 | 49762050 | NR3C2 | JASPAR | yes | 120774230 | ||
| chr12 | 49762045 | 49762060 | MEF2A | JASPAR | yes | 82400385 | ||
| chr12 | 49762045 | 49762060 | MEF2A | JASPAR | yes | 120774231 | ||
| chr12 | 49762046 | 49762058 | MEF2A | JASPAR | yes | 82400386 | ||
| chr12 | 49762046 | 49762058 | MEF2B | JASPAR | yes | 82400387 | ||
| chr12 | 49762046 | 49762058 | MEF2A | JASPAR | yes | 120774232 | ||
| chr12 | 49762046 | 49762058 | MEF2B | JASPAR | yes | 120774233 | ||
| chr12 | 49762047 | 49762057 | MEF2A | JASPAR | yes | 82400388 | ||
| chr12 | 49762047 | 49762057 | MEF2A | JASPAR | yes | 120774234 | ||
| chr12 | 49762054 | 49762065 | PHOX2A | JASPAR | yes | 82400389 | ||
| chr12 | 49762054 | 49762065 | PROP1 | JASPAR | yes | 82400390 | ||
| chr12 | 49762054 | 49762065 | PHOX2A | JASPAR | yes | 120774235 | ||
| chr12 | 49762054 | 49762065 | PROP1 | JASPAR | yes | 120774236 | ||
| chr12 | 49762074 | 49762078 | YY1 | TRANSFAC | yes | 82400391 | ||
| chr12 | 49762074 | 49762078 | YY1 | TRANSFAC | yes | 120774237 | ||
| chr12 | 49762075 | 49762085 | HOXB13 | JASPAR | yes | 82400392 | ||
| chr12 | 49762075 | 49762085 | HOXD13 | JASPAR | yes | 82400393 | ||
| chr12 | 49762075 | 49762085 | HOXB13 | JASPAR | yes | 120774238 | ||
| chr12 | 49762075 | 49762085 | HOXD13 | JASPAR | yes | 120774239 | ||
| chr12 | 49762075 | 49762086 | HOXA10 | JASPAR | yes | 82400394 | ||
| chr12 | 49762075 | 49762086 | HOXA10 | JASPAR | yes | 120774240 | ||
| chr12 | 49762078 | 49762088 | CUX1 | JASPAR | yes | 82400395 | ||
| chr12 | 49762078 | 49762088 | CUX2 | JASPAR | yes | 82400396 | ||
| chr12 | 49762078 | 49762088 | CUX1 | JASPAR | yes | 120774241 | ||
| chr12 | 49762078 | 49762088 | CUX2 | JASPAR | yes | 120774242 | ||
| chr12 | 49762085 | 49762105 | TP53 | JASPAR | yes | 82400397 | ||
| chr12 | 49762085 | 49762105 | TP53 | JASPAR | yes | 120774243 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr12 | 49762022 | rs534576103 | C | G,T |
|
2620929 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12 | 49687035 | 49692465 | + | PRPH | ENSG00000135406.9 | 49687035 | 0.95 | 1.0 | 12026 | 25024 | |
| chr12 | 49717019 | 49725514 | + | TROAP | ENSG00000135451.8 | 49717019 | 0.92 | 1.0 | 12027 | 55008 | |
| chr12 | 49726200 | 49730971 | - | C1QL4 | ENSG00000186897.3 | 49730971 | 0.97 | 1.0 | 12028 | 68960 | |
| chr12 | 49740700 | 49751309 | + | DNAJC22 | ENSG00000178401.10 | 49740700 | 0.96 | 1.0 | 12029 | 78689 | |
| chr12 | 49760367 | 49921205 | + | SPATS2 | ENSG00000123352.13 | 49760367 | 0.77 | 1.0 | 12030 | 98356 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|