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 |
---|---|---|---|---|---|---|---|---|
chr17 | 41242221 | 41242236 | RUNX2 | JASPAR | yes | 21241231 | ||
chr17 | 41242229 | 41242244 | TFAP2A | JASPAR | yes | 21241232 | ||
chr17 | 41242229 | 41242244 | TFAP2C | JASPAR | yes | 21241233 | ||
chr17 | 41242230 | 41242241 | TFAP2A | JASPAR | yes | 21241234 | ||
chr17 | 41242230 | 41242241 | TFAP2B | JASPAR | yes | 21241235 | ||
chr17 | 41242230 | 41242241 | TFAP2C | JASPAR | yes | 21241236 | ||
chr17 | 41242304 | 41242310 | JUN | TRANSFAC | yes | 21241237 | ||
chr17 | 41242308 | 41242329 | ZNF263 | JASPAR | yes | 21241238 | ||
chr17 | 41242309 | 41242322 | ZBTB18 | JASPAR | yes | 21241239 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 41242285 | rs2070834 | T | G | no | 4881402 | |
chr17 | 41242299 | rs532235452 | G | A | no | 4881403 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr17 | 41150290 | 41154976 | + | RPL27 | ENSG00000131469.8 | 41150290 | 0.8 | 1.0 | 15889 | 8083 | |
chr17 | 41158742 | 41166473 | + | IFI35 | ENSG00000068079.3 | 41158742 | 0.61 | 1.0 | 15890 | 16535 | |
chr17 | 41166622 | 41177140 | - | VAT1 | ENSG00000108828.11 | 41177140 | 0.71 | 1.0 | 15891 | 34933 | |
chr17 | 41177258 | 41184057 | + | RND2 | ENSG00000108830.7 | 41177258 | 0.89 | 0.98 | 15892 | 35051 | |
chr17 | 41196312 | 41277500 | - | BRCA1 | ENSG00000012048.15 | 41277500 | 0.9 | 0.98 | 15893 | 64834 | |
chr17 | 41322498 | 41363708 | + | NBR1 | ENSG00000188554.9 | 41322498 | 0.63 | 0.99 | 15894 | 19836 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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