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 | 49198510 | 49198514 | LFA1 | TRANSFAC | yes | 82399537 | ||
chr12 | 49198516 | 49198522 | JUN | TRANSFAC | yes | 82399538 | ||
chr12 | 49198519 | 49198534 | FOXA1 | JASPAR | yes | 82399539 | ||
chr12 | 49198520 | 49198532 | FOXI1 | JASPAR | yes | 82399540 | ||
chr12 | 49198521 | 49198533 | FOXC2 | JASPAR | yes | 82399541 | ||
chr12 | 49198522 | 49198533 | FOXB1 | JASPAR | yes | 82399542 | ||
chr12 | 49198522 | 49198533 | FOXC1 | JASPAR | yes | 82399543 | ||
chr12 | 49198523 | 49198527 | YY1 | TRANSFAC | yes | 82399544 | ||
chr12 | 49198527 | 49198531 | YY1 | TRANSFAC | yes | 82399545 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
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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 | 49082247 | 49110681 | - | CCNT1 | ENSG00000129315.5 | 49110681 | 0.63 | 0.99 | 12004 | 12182 | |
chr12 | 49121218 | 49159569 | + | LINC00935 | ENSG00000257987.1 | 49121218 | 0.99 | 0.0 | 12005 | 22719 | |
chr12 | 49159975 | 49182820 | - | ADCY6 | ENSG00000174233.7 | 49182820 | 0.78 | 1.0 | 12006 | 84321 | |
chr12 | 49207577 | 49222724 | + | CACNB3 | ENSG00000167535.3 | 49207577 | 0.84 | 1.0 | 12007 | 90965 | |
chr12 | 49223547 | 49246625 | - | DDX23 | ENSG00000174243.5 | 49246625 | 0.64 | 0.99 | 12008 | 51917 | |
chr12 | 49250928 | 49259681 | - | RND1 | ENSG00000172602.5 | 49259681 | 0.92 | 0.99 | 12009 | 38861 | |
chr12 | 49297893 | 49325623 | + | CCDC65 | ENSG00000139537.6 | 49297893 | 0.93 | 1.0 | 12011 | 649 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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