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 | 70103652 | 70103667 | NR2C2 | JASPAR | yes | 21287029 | ||
chr17 | 70103684 | 70103690 | ETS1 | JASPAR | yes | 21287030 | ||
chr17 | 70103689 | 70103705 | ZNF143 | JASPAR | yes | 21287031 | ||
chr17 | 70103694 | 70103700 | SOX10 | JASPAR | yes | 21287032 | ||
chr17 | 70103708 | 70103724 | RFX2 | JASPAR | yes | 21287033 | ||
chr17 | 70103708 | 70103724 | RFX3 | JASPAR | yes | 21287034 | ||
chr17 | 70103708 | 70103724 | RFX4 | JASPAR | yes | 21287035 | ||
chr17 | 70103709 | 70103728 | RFX2 | JASPAR | yes | 21287036 | ||
chr17 | 70103710 | 70103715 | GATA2 | JASPAR | yes | 21287037 | ||
chr17 | 70103723 | 70103729 | SOX10 | JASPAR | yes | 21287038 | ||
chr17 | 70103727 | 70103742 | RUNX2 | JASPAR | yes | 21287039 | ||
chr17 | 70103772 | 70103777 | ETS2 | TRANSFAC | yes | 21287040 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 70103751 | rs16977084 | C | T | no | 5031247 | |
chr17 | 70103773 | rs146388912 | G | A |
|
5031248 |
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 | 70036164 | 70036872 | + | AC007461.1 | ENSG00000267893.1 | 70036164 | 0.93 | 0.97 | 16198 | 32516 | |
chr17 | 70117161 | 70122561 | + | SOX9 | ENSG00000125398.5 | 70117161 | 0.81 | 1.0 | 16199 | 86619 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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