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
chr18 78011033 78011039 ESR1 TRANSFAC yes 111851064

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr18 78011040 rs73496421 A T no 5362620
chr18 78011085 rs137880551 G A no 5362621
chr18 78011126 rs539933226 C T no 5362622
chr18 78011244 rs577117283 T G no 5362623
chr18 78011266 rs544383201 A T no 5362624
chr18 78011282 rs143925609 A C no 5362625
chr18 78011356 rs541487299 G A no 5362626
chr18 78011381 rs560076005 T C no 5362627
chr18 78011548 rs148561871 G A no 5362628
chr18 78011583 rs142909940 C T no 5362629
chr18 78011689 rs146122648 T A no 5362630
chr18 78011946 rs113036875 A G no 5362631
chr18 78011962 rs531271021 C A,G no 5362632
chr18 78011963 rs3885673 T A,G no 5362633
chr18 78012012 rs191293055 G A no 5362634
chr18 78012048 rs143886728 C T no 5362635
chr18 78012217 rs151255665 G A no 5362636
chr18 78012249 rs7505302 G A no 5362637
chr18 78012343 rs116928938 G A no 5362638
chr18 78012344 rs571975839 G A no 5362639
chr18 78012418 rs191893226 C A no 5362640
chr18 78012463 rs72980401 G A no 5362641
chr18 78012466 rs375166798 C A no 5362642
chr18 78012557 rs574188338 G A no 5362643
chr18 78012683 rs116826391 A G no 5362644
chr18 78012684 rs114727542 T G no 5362645
chr18 78012691 rs79014523 C G no 5362646
chr18 78012833 rs77790030 C T no 5362647
chr18 78012849 rs80299001 C G,T no 5362648
chr18 78012915 rs73496422 G T no 5362649
chr18 78012929 rs11874613 C A no 5362650
chr18 78013053 rs113996024 G A no 5362651
chr18 78013063 rs578259624 G A no 5362652
chr18 78013325 rs73496426 G A no 5362653
chr18 78013450 rs544282627 GT G no 5362654
chr18 78013461 rs180730520 G T no 5362655
chr18 78013563 rs150014135 A G no 5362656
chr18 78013684 rs374973509 C G no 5362657
chr18 78013806 rs142428722 C T no 5362658
chr18 78013843 rs181324045 C T no 5362659
chr18 78013878 rs12954011 G A no 5362660
chr18 78014091 rs187084031 T A no 5362661
chr18 78014205 rs115503032 A T no 5362662
chr18 78014213 rs35708369 T C no 5362663
chr18 78014320 rs12606550 C T no 5362664
chr18 78014335 rs561758325 TG T no 5362665
chr18 78014346 rs76440299 G A no 5362666
chr18 78014365 rs146185798 C CATCA no 5362667
chr18 78014365 rs55675166 C CATCA no 5362668
chr18 78014427 rs80204604 T A,C no 5362669
chr18 78014528 rs571271151 TTCTTTCTTTC T no 5362670
chr18 78014582 rs12456851 C A,T no 5362671
chr18 78014607 rs191147511 C T no 5362672
chr18 78014608 rs8099569 G A no 5362673
chr18 78014610 rs367831929 A G no 5362674
chr18 78014614 rs7507083 G A no 5362675
chr18 78014624 rs116516641 G A,T no 5362676
chr18 78014690 rs143587518 G A no 5362677
chr18 78014821 rs186957479 A G no 5362678
chr18 78014888 rs115844861 G A no 5362679
chr18 78014997 rs12959193 G C no 5362680
chr18 78015019 rs376162359 C T no 5362681
chr18 78015020 rs141606675 G A no 5362682
chr18 78015057 rs7236400 T C no 5362683
chr18 78015180 rs12960632 C T no 5362684
chr18 78015188 rs79220548 G A no 5362685

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance between enhancer and TSS id More
chr18 77915115 78005429 - PARD6G ENSG00000178184.11 78005429 0.82 1.0 16695 94402


Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results