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 | 49371075 | 49371093 | ESR1 | JASPAR | yes | 82399721 | ||
| chr12 | 49371118 | 49371130 | E2F8 | JASPAR | yes | 82399722 | ||
| chr12 | 49371126 | 49371130 | H1TF2 | TRANSFAC | yes | 82399723 | ||
| chr12 | 49371126 | 49371130 | NFE | TRANSFAC | yes | 82399724 | ||
| chr12 | 49371126 | 49371130 | SRF | TRANSFAC | yes | 82399725 | ||
| chr12 | 49371144 | 49371156 | PKNOX2 | JASPAR | yes | 82399726 | ||
| chr12 | 49371144 | 49371156 | TGIF2 | JASPAR | yes | 82399727 | ||
| chr12 | 49371147 | 49371157 | TEAD1 | JASPAR | yes | 82399728 | ||
| chr12 | 49371147 | 49371157 | TEAD4 | JASPAR | yes | 82399729 | ||
| chr12 | 49371147 | 49371159 | TEAD1 | JASPAR | yes | 82399730 | ||
| chr12 | 49371160 | 49371174 | CREB3 | JASPAR | yes | 82399731 | ||
| chr12 | 49371182 | 49371197 | HNF4G | JASPAR | yes | 82399732 | ||
| chr12 | 49371183 | 49371197 | RXRG | JASPAR | yes | 82399733 | ||
| chr12 | 49371183 | 49371198 | HNF4A | JASPAR | yes | 82399734 | ||
| chr12 | 49371187 | 49371193 | SOX10 | JASPAR | yes | 82399735 | ||
| chr12 | 49371192 | 49371196 | LFA1 | TRANSFAC | yes | 82399736 | ||
| chr12 | 49371213 | 49371227 | POU4F1 | JASPAR | yes | 82399737 | ||
| chr12 | 49371213 | 49371229 | POU4F2 | JASPAR | yes | 82399738 | ||
| chr12 | 49371218 | 49371222 | YY1 | TRANSFAC | yes | 82399739 | ||
| chr12 | 49371227 | 49371248 | ZNF263 | JASPAR | yes | 82399740 | ||
| chr12 | 49371232 | 49371242 | MAX | JASPAR | yes | 82399741 | ||
| chr12 | 49371233 | 49371244 | NRF1 | JASPAR | yes | 82399742 | ||
| chr12 | 49371239 | 49371260 | ZNF263 | JASPAR | yes | 82399743 | ||
| chr12 | 49371244 | 49371250 | ZNF354C | JASPAR | yes | 82399744 | ||
| chr12 | 49371248 | 49371268 | RREB1 | JASPAR | yes | 82399745 | ||
| chr12 | 49371263 | 49371273 | SMAD3 | JASPAR | yes | 82399746 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr12 | 49371130 | rs532646420 | A | G |
|
2618817 | |
| chr12 | 49371237 | rs190123578 | A | C |
|
2618818 |
| 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 | 49297286 | 49351148 | - | RP11-302B13.5 | ENSG00000272822.1 | 49351148 | 0.92 | 0.92 | 12010 | 80083 | |
| chr12 | 49297893 | 49325623 | + | CCDC65 | ENSG00000139537.6 | 49297893 | 0.93 | 1.0 | 12011 | 26828 | |
| chr12 | 49315301 | 49320257 | - | FKBP11 | ENSG00000134285.6 | 49320257 | 0.91 | 0.99 | 12012 | 49192 | |
| chr12 | 49315767 | 49333446 | - | AC073610.5 | ENSG00000255863.1 | 49333446 | 1.0 | 0.99 | 12013 | 62381 | |
| chr12 | 49329506 | 49351334 | - | ARF3 | ENSG00000134287.5 | 49351334 | 0.76 | 0.99 | 12014 | 80269 | |
| chr12 | 49359123 | 49365546 | - | WNT10B | ENSG00000169884.9 | 49365546 | 0.86 | 1.0 | 12015 | 94481 | |
| chr12 | 49372398 | 49375459 | + | WNT1 | ENSG00000125084.7 | 49372398 | 0.93 | 1.0 | 12016 | 98889 | |
| chr12 | 49388932 | 49393092 | - | DDN | ENSG00000181418.7 | 49393092 | 1.0 | 1.0 | 12017 | 78195 | |
| chr12 | 49396057 | 49412980 | - | PRKAG1 | ENSG00000181929.7 | 49412980 | 0.61 | 1.0 | 12018 | 58307 | |
| chr12 | 49412758 | 49453557 | - | KMT2D | ENSG00000167548.10 | 49453557 | 0.66 | 1.0 | 12019 | 17730 | |
| chr12 | 49458468 | 49463808 | - | RHEBL1 | ENSG00000167550.6 | 49463808 | 0.9 | 1.0 | 12020 | 7479 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|