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 | 43863424 | 43863436 | GRHL1 | JASPAR | yes | 21246011 | ||
chr17 | 43863425 | 43863435 | TFCP2 | JASPAR | yes | 21246012 | ||
chr17 | 43863460 | 43863466 | TCF1 | TRANSFAC | yes | 21246013 | ||
chr17 | 43863477 | 43863498 | IRF1 | JASPAR | yes | 21246014 | ||
chr17 | 43863478 | 43863493 | FOXP1 | JASPAR | yes | 21246015 | ||
chr17 | 43863478 | 43863499 | IRF1 | JASPAR | yes | 21246016 | ||
chr17 | 43863479 | 43863490 | FOXP2 | JASPAR | yes | 21246017 | ||
chr17 | 43863479 | 43863494 | STAT2 | JASPAR | yes | 21246018 | ||
chr17 | 43863481 | 43863492 | FOXA1 | JASPAR | yes | 21246019 | ||
chr17 | 43863482 | 43863503 | IRF1 | JASPAR | yes | 21246020 | ||
chr17 | 43863483 | 43863498 | FOXP1 | JASPAR | yes | 21246021 | ||
chr17 | 43863483 | 43863504 | IRF1 | JASPAR | yes | 21246022 | ||
chr17 | 43863488 | 43863503 | FOXP1 | JASPAR | yes | 21246023 | ||
chr17 | 43863490 | 43863505 | FOXP1 | JASPAR | yes | 21246024 | ||
chr17 | 43863492 | 43863507 | FOXP1 | JASPAR | yes | 21246025 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 43863405 | rs533376567 | C | G,T | no | 4897353 | |
chr17 | 43863421 | rs116551317 | T | C | no | 4897354 | |
chr17 | 43863493 | rs66781068 | C | CT,CTT |
|
4897355 | |
chr17 | 43863493 | rs66923759 | C | CT |
|
4897356 |
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 | 43922256 | 43924438 | + | SPPL2C | ENSG00000185294.5 | 43922256 | 0.97 | 0.0 | 15953 | 41251 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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