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 | 5412378 | 5412393 | RFX5 | JASPAR | yes | 21189315 | ||
chr17 | 5412378 | 5412393 | RFX5 | JASPAR | yes | 52874358 | ||
chr17 | 5412398 | 5412401 | MYB | TRANSFAC | yes | 21189316 | ||
chr17 | 5412398 | 5412401 | MYB | TRANSFAC | yes | 52874359 | ||
chr17 | 5412399 | 5412409 | MYF6 | JASPAR | yes | 21189317 | ||
chr17 | 5412399 | 5412409 | MYF6 | JASPAR | yes | 52874360 | ||
chr17 | 5412401 | 5412420 | RFX2 | JASPAR | yes | 21189318 | ||
chr17 | 5412401 | 5412420 | RFX2 | JASPAR | yes | 52874361 | ||
chr17 | 5412403 | 5412418 | RFX5 | JASPAR | yes | 21189319 | ||
chr17 | 5412403 | 5412418 | RFX5 | JASPAR | yes | 52874362 | ||
chr17 | 5412404 | 5412409 | MYC | TRANSFAC | yes | 21189320 | ||
chr17 | 5412404 | 5412409 | MYC | TRANSFAC | yes | 52874363 | ||
chr17 | 5412404 | 5412421 | BCL6B | JASPAR | yes | 21189321 | ||
chr17 | 5412404 | 5412421 | BCL6B | JASPAR | yes | 52874364 | ||
chr17 | 5412405 | 5412420 | STAT1 | JASPAR | yes | 21189322 | ||
chr17 | 5412405 | 5412420 | STAT1 | JASPAR | yes | 52874365 | ||
chr17 | 5412407 | 5412418 | STAT1 | JASPAR | yes | 21189323 | ||
chr17 | 5412407 | 5412418 | STAT3 | JASPAR | yes | 21189324 | ||
chr17 | 5412407 | 5412418 | STAT1 | JASPAR | yes | 52874366 | ||
chr17 | 5412407 | 5412418 | STAT3 | JASPAR | yes | 52874367 | ||
chr17 | 5412442 | 5412446 | H1TF2 | TRANSFAC | yes | 21189325 | ||
chr17 | 5412442 | 5412446 | NFE | TRANSFAC | yes | 21189326 | ||
chr17 | 5412442 | 5412446 | SRF | TRANSFAC | yes | 21189327 | ||
chr17 | 5412442 | 5412446 | H1TF2 | TRANSFAC | yes | 52874368 | ||
chr17 | 5412442 | 5412446 | NFE | TRANSFAC | yes | 52874369 | ||
chr17 | 5412442 | 5412446 | SRF | TRANSFAC | yes | 52874370 | ||
chr17 | 5412442 | 5412448 | NFYC | TRANSFAC | yes | 21189328 | ||
chr17 | 5412442 | 5412448 | NFYC | TRANSFAC | yes | 52874371 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 5412473 | rs8079727 | A | C,T | no | 4718863 | |
chr17 | 5412477 | rs146181309 | C | T | no | 4718864 | |
chr17 | 5412490 | rs189485366 | C | T | no | 4718865 |
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 | 5264258 | 5323480 | - | NUP88 | ENSG00000108559.7 | 5323480 | 0.8 | 1.0 | 15310 | 11101 | |
chr17 | 5322961 | 5336196 | + | RPAIN | ENSG00000129197.10 | 5322961 | 0.69 | 1.0 | 15311 | 10582 | |
chr17 | 5336097 | 5352150 | - | C1QBP | ENSG00000108561.4 | 5352150 | 0.89 | 0.99 | 15312 | 39771 | |
chr17 | 5344232 | 5372380 | - | DHX33 | ENSG00000005100.8 | 5372380 | 0.62 | 0.99 | 15313 | 60001 | |
chr17 | 5374571 | 5390131 | - | DERL2 | ENSG00000072849.6 | 5390131 | 0.77 | 0.99 | 15314 | 77752 | |
chr17 | 5389605 | 5394134 | + | MIS12 | ENSG00000167842.11 | 5389605 | 0.66 | 0.99 | 15315 | 77226 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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