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 |
---|---|---|---|---|---|---|---|---|
chr1 | 166102453 | 166102907 | CTCF | UCSC Txn Factor | no | Conserved | 107843197 | |
chr1 | 166102836 | 166102851 | FOXP1 | JASPAR | yes | 118391303 | ||
chr1 | 166102837 | 166102843 | TBP | TRANSFAC | yes | 118391304 | ||
chr1 | 166102838 | 166102853 | FOXP1 | JASPAR | yes | 118391305 | ||
chr1 | 166102838 | 166102859 | IRF1 | JASPAR | yes | 118391306 | ||
chr1 | 166102850 | 166102864 | FOXF2 | JASPAR | yes | 118391307 | ||
chr1 | 166102860 | 166102864 | TEAD2 | TRANSFAC | yes | 118391308 | ||
chr1 | 166102896 | 166102902 | HiNF-A | TRANSFAC | yes | 118391309 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr1 | 166102838 | rs199770987 | T | TA,TAA |
|
696621 | |
chr1 | 166102838 | rs5778486 | T | TA,TAA,TAAA |
|
696622 | |
chr1 | 166102861 | rs572075103 | T | C |
|
696623 | |
chr1 | 166102885 | rs61835123 | T | C |
|
696624 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr1 | 166026674 | 166136206 | - | FAM78B | ENSG00000188859.5 | 166136206 | 0.8 | 1.0 | 1521 | 66707 | |
chr1 | 166026679 | 166028709 | - | AL626787.1 | ENSG00000267884.1 | 166028709 | 0.95 | 0.94 | 1522 | 25873 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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