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 |
---|---|---|---|---|---|---|---|---|
chr14 | 75492533 | 75492554 | ZNF263 | JASPAR | yes | 107582379 | ||
chr14 | 75492533 | 75492554 | ZNF263 | JASPAR | yes | 116598786 | ||
chr14 | 75492555 | 75492563 | MEIS2 | JASPAR | yes | 107582380 | ||
chr14 | 75492555 | 75492563 | MEIS2 | JASPAR | yes | 116598787 | ||
chr14 | 75492556 | 75492560 | NFE | TRANSFAC | yes | 107582381 | ||
chr14 | 75492556 | 75492560 | NFE | TRANSFAC | yes | 116598788 | ||
chr14 | 75492556 | 75492563 | MEIS1 | JASPAR | yes | 107582382 | ||
chr14 | 75492556 | 75492563 | MEIS1 | JASPAR | yes | 116598789 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr14 | 75492532 | rs562852222 | G | T | no | 3663758 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr14 | 75408537 | 75422487 | - | PGF | ENSG00000119630.9 | 75422487 | 0.9 | 1.0 | 13488 | 29964 | |
chr14 | 75469614 | 75476292 | + | EIF2B2 | ENSG00000119718.6 | 75469614 | 0.66 | 1.0 | 13489 | 77091 | |
chr14 | 75480467 | 75518235 | - | MLH3 | ENSG00000119684.11 | 75518235 | 0.68 | 0.99 | 13490 | 74322 | |
chr14 | 75519924 | 75536186 | - | ACYP1 | ENSG00000119640.4 | 75536186 | 0.76 | 1.0 | 13491 | 56371 | |
chr14 | 75530873 | 75545126 | + | ZC2HC1C | ENSG00000119703.12 | 75530873 | 0.84 | 0.99 | 13492 | 61684 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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