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 |
---|---|---|---|---|---|---|---|---|
chr3 | 49503178 | 49503184 | PEA3 | TRANSFAC | yes | 70980115 | ||
chr3 | 49503187 | 49503202 | STAT1 | JASPAR | yes | 70980116 | ||
chr3 | 49503189 | 49503200 | STAT1 | JASPAR | yes | 70980117 | ||
chr3 | 49503189 | 49503200 | STAT3 | JASPAR | yes | 70980118 | ||
chr3 | 49503190 | 49503198 | STAT6 | TRANSFAC | yes | 70980119 | ||
chr3 | 49503194 | 49503199 | ETS2 | TRANSFAC | yes | 70980120 | ||
chr3 | 49503212 | 49503224 | FOXI1 | JASPAR | yes | 70980121 | ||
chr3 | 49503225 | 49503234 | THAP1 | JASPAR | yes | 70980122 | ||
chr3 | 49503233 | 49503241 | GATA3 | JASPAR | yes | 70980123 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr3 | 49503155 | rs13086658 | G | T | no | 6725908 | |
chr3 | 49503166 | rs73073015 | G | A | no | 6725909 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr3 | 49396578 | 49450431 | - | RHOA | ENSG00000067560.6 | 49450431 | 0.61 | 1.0 | 3672 | 47277 | |
chr3 | 49449639 | 49453908 | + | TCTA | ENSG00000145022.4 | 49449639 | 0.73 | 0.99 | 3673 | 46485 | |
chr3 | 49454211 | 49460186 | - | AMT | ENSG00000145020.10 | 49460186 | 0.69 | 1.0 | 3674 | 57032 | |
chr3 | 49460379 | 49466759 | - | NICN1 | ENSG00000145029.7 | 49466759 | 0.66 | 1.0 | 3675 | 63605 | |
chr3 | 49506146 | 49573048 | + | DAG1 | ENSG00000173402.7 | 49506146 | 0.75 | 1.0 | 3676 | 97118 | |
chr3 | 49591922 | 49708978 | + | BSN | ENSG00000164061.4 | 49591922 | 0.85 | 0.99 | 3677 | 11342 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
---|