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 | 41723666 | 41723685 | CTCF | JASPAR | yes | 21241938 | ||
chr17 | 41723666 | 41723685 | CTCF | JASPAR | yes | 54363202 | ||
chr17 | 41723672 | 41723678 | SP1 | TRANSFAC | yes | 21241939 | ||
chr17 | 41723672 | 41723678 | SP1 | TRANSFAC | yes | 54363203 | ||
chr17 | 41723679 | 41723693 | TLX1 | JASPAR | yes | 21241940 | ||
chr17 | 41723679 | 41723693 | TLX1 | JASPAR | yes | 54363204 | ||
chr17 | 41723692 | 41723698 | MAZ | TRANSFAC | yes | 21241941 | ||
chr17 | 41723692 | 41723698 | MAZ | TRANSFAC | yes | 54363205 | ||
chr17 | 41723701 | 41723705 | ESR1 | TRANSFAC | yes | 21241942 | ||
chr17 | 41723701 | 41723705 | ESR1 | TRANSFAC | yes | 54363206 | ||
chr17 | 41723717 | 41723727 | RELA | JASPAR | yes | 21241943 | ||
chr17 | 41723717 | 41723727 | RELA | JASPAR | yes | 54363207 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 41723720 | rs561310282 | G | C |
|
4885068 | |
chr17 | 41723752 | rs76958397 | C | G | no | 4885069 | |
chr17 | 41723794 | rs145436891 | C | T | no | 4885070 |
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 | 41605212 | 41656988 | - | ETV4 | ENSG00000175832.8 | 41656988 | 0.94 | 0.99 | 15898 | 33319 | |
chr17 | 41717756 | 41739322 | - | MEOX1 | ENSG00000005102.8 | 41739322 | 0.9 | 0.95 | 15899 | 84481 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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