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 |
---|---|---|---|---|---|---|---|---|
chr11 | 61690524 | 61691563 | POLR2A | UCSC Txn Factor | no | Conserved | 107973074 | |
chr11 | 61690837 | 61690858 | MAFG | JASPAR | yes | 114079037 | ||
chr11 | 61690843 | 61690847 | NFE | TRANSFAC | yes | 114079038 | ||
chr11 | 61690843 | 61690848 | GATA1 | TRANSFAC | yes | 114079039 | ||
chr11 | 61690843 | 61690849 | GATA3 | JASPAR | yes | 114079040 | ||
chr11 | 61690855 | 61690876 | ZNF263 | JASPAR | yes | 114079041 | ||
chr11 | 61690876 | 61690895 | REST | JASPAR | yes | 114079042 | ||
chr11 | 61690889 | 61690900 | NFE2L2 | JASPAR | yes | 114079043 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr11 | 61690829 | rs192358410 | C | T |
|
2027580 | |
chr11 | 61690901 | rs7927548 | G | A |
|
2027581 | |
chr11 | 61690918 | rs143605816 | G | A |
|
2027582 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr11 | 61567099 | 61596790 | - | FADS1 | ENSG00000149485.12 | 61596790 | 0.74 | 0.99 | 10946 | 5974 | |
chr11 | 61640991 | 61659523 | - | FADS3 | ENSG00000221968.4 | 61659523 | 0.7 | 1.0 | 10947 | 68707 | |
chr11 | 61664773 | 61687741 | - | RAB3IL1 | ENSG00000167994.7 | 61687741 | 0.81 | 1.0 | 10948 | 96925 | |
chr11 | 61717293 | 61732987 | + | BEST1 | ENSG00000167995.11 | 61717293 | 0.82 | 1.0 | 10949 | 73654 | |
chr11 | 61727190 | 61735132 | - | FTH1 | ENSG00000167996.11 | 61735132 | 0.62 | 0.99 | 10950 | 55815 | |
chr11 | 61735453 | 61736755 | + | AP003733.1 | ENSG00000269089.1 | 61735453 | 0.8 | 1.0 | 10951 | 55494 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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