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 |
---|---|---|---|---|---|---|---|---|
chr12 | 95836268 | 95836280 | INSM1 | JASPAR | yes | 82459989 | ||
chr12 | 95836268 | 95836280 | INSM1 | JASPAR | yes | 122997832 | ||
chr12 | 95836268 | 95836282 | NR2F1 | JASPAR | yes | 82459990 | ||
chr12 | 95836268 | 95836282 | NR2F1 | JASPAR | yes | 122997833 | ||
chr12 | 95836316 | 95836321 | MYC | TRANSFAC | yes | 82459991 | ||
chr12 | 95836316 | 95836321 | MYC | TRANSFAC | yes | 122997834 | ||
chr12 | 95836317 | 95836328 | FOXH1 | JASPAR | yes | 82459992 | ||
chr12 | 95836317 | 95836328 | FOXH1 | JASPAR | yes | 122997835 | ||
chr12 | 95836320 | 95836331 | DUX4 | JASPAR | yes | 82459993 | ||
chr12 | 95836320 | 95836331 | DUX4 | JASPAR | yes | 122997836 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr12 | 95836322 | rs2769459 | G | A |
|
2826799 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr12 | 95770984 | 95774672 | - | RP11-167N24.6 | ENSG00000258247.1 | 95774672 | 0.95 | 0.0 | 12416 | 38436 | |
chr12 | 95867296 | 95909615 | + | METAP2 | ENSG00000111142.9 | 95867296 | 0.65 | 0.99 | 12417 | 69050 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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