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 | 27116094 | 27116109 | FOXP1 | JASPAR | yes | 21214043 | ||
chr17 | 27116095 | 27116110 | FOXP1 | JASPAR | yes | 21214044 | ||
chr17 | 27116096 | 27116111 | FOXP1 | JASPAR | yes | 21214045 | ||
chr17 | 27116097 | 27116112 | FOXP1 | JASPAR | yes | 21214046 | ||
chr17 | 27116098 | 27116113 | FOXP1 | JASPAR | yes | 21214047 | ||
chr17 | 27116099 | 27116114 | FOXP1 | JASPAR | yes | 21214048 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
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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 | 27030215 | 27038872 | - | PROCA1 | ENSG00000167525.9 | 27038872 | 0.79 | 0.98 | 15582 | 22779 | |
chr17 | 27041299 | 27045447 | - | RAB34 | ENSG00000109113.13 | 27045447 | 0.72 | 0.96 | 15583 | 29354 | |
chr17 | 27046411 | 27051377 | + | RPL23A | ENSG00000198242.9 | 27046411 | 0.83 | 1.0 | 15584 | 30318 | |
chr17 | 27051366 | 27054953 | - | TLCD1 | ENSG00000160606.6 | 27054953 | 0.83 | 1.0 | 15585 | 38860 | |
chr17 | 27052915 | 27070473 | + | NEK8 | ENSG00000160602.9 | 27052915 | 0.79 | 1.0 | 15586 | 36822 | |
chr17 | 27071002 | 27077974 | + | TRAF4 | ENSG00000076604.10 | 27071002 | 0.83 | 1.0 | 15587 | 54909 | |
chr17 | 27082996 | 27182250 | - | FAM222B | ENSG00000173065.9 | 27182250 | 0.67 | 1.0 | 15588 | 33864 | |
chr17 | 27181956 | 27188085 | + | ERAL1 | ENSG00000132591.7 | 27181956 | 0.66 | 0.99 | 15589 | 34158 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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