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 |
---|---|---|---|---|---|---|---|---|
chr11 | 63262898 | 63262904 | TCF4 | TRANSFAC | yes | 114081815 | ||
chr11 | 63262917 | 63262936 | RFX2 | JASPAR | yes | 114081816 | ||
chr11 | 63262920 | 63262924 | NFE | TRANSFAC | yes | 114081817 | ||
chr11 | 63262921 | 63262937 | RFX2 | JASPAR | yes | 114081818 | ||
chr11 | 63262921 | 63262937 | RFX3 | JASPAR | yes | 114081819 | ||
chr11 | 63262921 | 63262937 | RFX4 | JASPAR | yes | 114081820 | ||
chr11 | 63262921 | 63262937 | RFX5 | JASPAR | yes | 114081821 | ||
chr11 | 63262922 | 63262941 | RFX2 | JASPAR | yes | 114081822 | ||
chr11 | 63262931 | 63262946 | RUNX2 | JASPAR | yes | 114081823 | ||
chr11 | 63262943 | 63262949 | SOX10 | JASPAR | yes | 114081824 | ||
chr11 | 63262961 | 63262980 | REST | JASPAR | yes | 114081825 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr11 | 63262908 | rs76336514 | C | T | no | 2034205 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr11 | 63228876 | 63258666 | - | HRASLS5 | ENSG00000168004.5 | 63258666 | 0.93 | 0.93 | 10997 | 95791 | |
chr11 | 63273556 | 63284246 | + | LGALS12 | ENSG00000133317.10 | 63273556 | 0.99 | 1.0 | 10998 | 89435 | |
chr11 | 63304281 | 63313934 | + | RARRES3 | ENSG00000133321.6 | 63304281 | 0.8 | 0.92 | 10999 | 58710 | |
chr11 | 63320242 | 63330855 | - | HRASLS2 | ENSG00000133328.3 | 63330855 | 0.84 | 0.99 | 11000 | 32136 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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