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 | 41162770 | 41163160 | EP300 | UCSC Txn Factor | no | Conserved | 108261068 | |
chr17 | 41162914 | 41162929 | RUNX2 | JASPAR | yes | 21241028 | ||
chr17 | 41162915 | 41162918 | MYB | TRANSFAC | yes | 21241029 | ||
chr17 | 41162915 | 41162924 | RUNX2 | JASPAR | yes | 21241030 | ||
chr17 | 41162915 | 41162932 | RARA | JASPAR | yes | 21241031 | ||
chr17 | 41162925 | 41162940 | HNF4A | JASPAR | yes | 21241032 | ||
chr17 | 41162926 | 41162941 | HNF4G | JASPAR | yes | 21241033 | ||
chr17 | 41162926 | 41162941 | NR2C2 | JASPAR | yes | 21241034 | ||
chr17 | 41162948 | 41162954 | SOX10 | JASPAR | yes | 21241035 | ||
chr17 | 41162957 | 41162961 | YY1 | TRANSFAC | yes | 21241036 | ||
chr17 | 41162957 | 41162967 | HOXB13 | JASPAR | yes | 21241037 | ||
chr17 | 41162967 | 41162972 | GATA2 | JASPAR | yes | 21241038 | ||
chr17 | 41162973 | 41162987 | STAT1 | JASPAR | yes | 21241039 | ||
chr17 | 41162974 | 41162986 | IRF1 | JASPAR | yes | 21241040 | ||
chr17 | 41162991 | 41163003 | JDP2 | JASPAR | yes | 21241041 | ||
chr17 | 41163022 | 41163035 | EOMES | JASPAR | yes | 21241042 | ||
chr17 | 41163024 | 41163035 | TBX20 | JASPAR | yes | 21241043 | ||
chr17 | 41163025 | 41163035 | TBX21 | JASPAR | yes | 21241044 | ||
chr17 | 41163026 | 41163034 | MGA | JASPAR | yes | 21241045 | ||
chr17 | 41163026 | 41163034 | TBX15 | JASPAR | yes | 21241046 | ||
chr17 | 41163026 | 41163034 | TBX1 | JASPAR | yes | 21241047 | ||
chr17 | 41163026 | 41163034 | TBX4 | JASPAR | yes | 21241048 | ||
chr17 | 41163026 | 41163034 | TBX5 | JASPAR | yes | 21241049 | ||
chr17 | 41163030 | 41163040 | SP1 | JASPAR | yes | 21241050 | ||
chr17 | 41163057 | 41163069 | TEAD1 | JASPAR | yes | 21241051 | ||
chr17 | 41163058 | 41163068 | NFATC3 | JASPAR | yes | 21241052 | ||
chr17 | 41163063 | 41163073 | TBX21 | JASPAR | yes | 21241053 | ||
chr17 | 41163063 | 41163074 | TBX2 | JASPAR | yes | 21241054 | ||
chr17 | 41163064 | 41163072 | MGA | JASPAR | yes | 21241055 | ||
chr17 | 41163064 | 41163072 | TBX15 | JASPAR | yes | 21241056 | ||
chr17 | 41163064 | 41163072 | TBX1 | JASPAR | yes | 21241057 | ||
chr17 | 41163064 | 41163072 | TBX4 | JASPAR | yes | 21241058 | ||
chr17 | 41163064 | 41163072 | TBX5 | JASPAR | yes | 21241059 | ||
chr17 | 41163064 | 41163074 | TBR1 | JASPAR | yes | 21241060 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 41162883 | rs144270397 | C | T |
|
4881136 |
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 | 41102543 | 41116515 | - | AARSD1 | ENSG00000266967.2 | 41116515 | 0.57 | 0.95 | 15886 | 53637 | |
chr17 | 41102543 | 41132545 | - | PTGES3L-AARSD1 | ENSG00000108825.13 | 41132545 | 0.83 | 0.88 | 15885 | 69667 | |
chr17 | 41120105 | 41132545 | - | PTGES3L | ENSG00000267060.1 | 41132545 | 0.92 | 0.98 | 15887 | 69667 | |
chr17 | 41132582 | 41145707 | + | RUNDC1 | ENSG00000198863.3 | 41132582 | 0.58 | 1.0 | 15888 | 69704 | |
chr17 | 41150290 | 41154976 | + | RPL27 | ENSG00000131469.8 | 41150290 | 0.8 | 1.0 | 15889 | 87412 | |
chr17 | 41158742 | 41166473 | + | IFI35 | ENSG00000068079.3 | 41158742 | 0.61 | 1.0 | 15890 | 95864 | |
chr17 | 41166622 | 41177140 | - | VAT1 | ENSG00000108828.11 | 41177140 | 0.71 | 1.0 | 15891 | 85934 | |
chr17 | 41177258 | 41184057 | + | RND2 | ENSG00000108830.7 | 41177258 | 0.89 | 0.98 | 15892 | 85816 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
---|