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 |
---|---|---|---|---|---|---|---|---|
chr16 | 85137134 | 85137362 | SPI1 | UCSC Txn Factor | no | Conserved | 108213339 | |
chr16 | 85137226 | 85137229 | MYB | TRANSFAC | yes | 49406871 | ||
chr16 | 85137236 | 85137257 | IRF1 | JASPAR | yes | 49406872 | ||
chr16 | 85137238 | 85137253 | STAT2 | JASPAR | yes | 49406873 | ||
chr16 | 85137239 | 85137253 | STAT1 | JASPAR | yes | 49406874 | ||
chr16 | 85137240 | 85137252 | IRF1 | JASPAR | yes | 49406875 | ||
chr16 | 85137240 | 85137254 | IRF7 | JASPAR | yes | 49406876 | ||
chr16 | 85137240 | 85137254 | IRF8 | JASPAR | yes | 49406877 | ||
chr16 | 85137240 | 85137255 | IRF9 | JASPAR | yes | 49406878 | ||
chr16 | 85137244 | 85137259 | STAT2 | JASPAR | yes | 49406879 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr16 | 85137235 | rs62049957 | G | A |
|
4616601 | |
chr16 | 85137251 | rs6564101 | T | C |
|
4616602 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr16 | 85007787 | 85045141 | - | ZDHHC7 | ENSG00000153786.8 | 85045141 | 0.63 | 0.99 | 15126 | 7915 | |
chr16 | 85061375 | 85127836 | + | KIAA0513 | ENSG00000135709.8 | 85061375 | 0.66 | 1.0 | 15127 | 24149 | |
chr16 | 85131965 | 85146114 | - | FAM92B | ENSG00000153789.8 | 85146114 | 0.98 | 1.0 | 15128 | 91182 | |
chr16 | 85204882 | 85218969 | + | CTC-786C10.1 | ENSG00000262601.1 | 85204882 | 0.8 | 1.0 | 15129 | 32414 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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