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 |
---|---|---|---|---|---|---|---|---|
chr1 | 8986053 | 8986059 | SOX10 | JASPAR | yes | 118226378 | ||
chr1 | 8986068 | 8986078 | ELK1 | JASPAR | yes | 118226379 | ||
chr1 | 8986070 | 8986081 | ELK4 | JASPAR | yes | 118226380 | ||
chr1 | 8986072 | 8986078 | ETS1 | JASPAR | yes | 118226381 | ||
chr1 | 8986078 | 8986082 | NFE | TRANSFAC | yes | 118226382 | ||
chr1 | 8986079 | 8986084 | GATA2 | JASPAR | yes | 118226383 | ||
chr1 | 8986096 | 8986099 | MYB | TRANSFAC | yes | 118226384 | ||
chr1 | 8986129 | 8986135 | NFIC | JASPAR | yes | 118226385 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr1 | 8986041 | rs140005761 | T | G | no | 60521 | |
chr1 | 8986048 | rs77375575 | T | C | no | 60522 | |
chr1 | 8986070 | rs143716957 | C | T |
|
60523 | |
chr1 | 8986124 | rs72859089 | A | C | no | 60524 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr1 | 8921061 | 8939308 | - | ENO1 | ENSG00000074800.9 | 8939308 | 0.77 | 1.0 | 117 | 53287 | |
chr1 | 9005926 | 9035151 | + | CA6 | ENSG00000131686.10 | 9005926 | 0.99 | 0.69 | 118 | 80213 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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