EnhancerDB
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Chromosome characteristics of ZNF274[chr13:111183656-111188794]
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Enhancers possibly regulated by ZNF274[chr13:111183656-111188794]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr13 111186805 111212195 enh15501
Prostate (PC-3) Liver (HepG2) Epithelial (MCF-7) Cervix (HeLa-S3) Brain (SK-N-SH) Esophagus Astrocyte Bone (Osteoblast) Stomach Placenta Colon (HCT116) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Lung (PC-9) Pancreas Spleen Neural Stem Cells (H9) Heart
chr13 111184119 111184417 vista17064
VISTA
chr13 111188602 111188989 vista17065
VISTA
SNP sites on ZNF274[chr13:111183656-111188794]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr13 111183707 rs562134191 C T 3395564
chr13 111183726 rs118064598 G T 3395565
chr13 111183780 rs548167152 G A,T 3395566
chr13 111183880 rs60748404 G A 3395567
chr13 111183915 rs568062040 G C 3395568
chr13 111183943 rs2025904 G A 3395569
chr13 111184042 rs186514249 G A 3395570
chr13 111184064 rs190185455 G A 3395571
chr13 111184171 rs142544553 T A 3395572
chr13 111184196 rs77995515 G A 3395573
chr13 111184213 rs140809235 G A 3395574
chr13 111184256 rs2025905 C G 3395575
chr13 111184283 rs533816635 G A 3395576
chr13 111184311 rs144925845 A G 3395577
chr13 111184364 rs116548274 T C,G 3395578
chr13 111184394 rs151244847 A AAG 3395579
chr13 111184426 rs146756258 G A 3395580
chr13 111184433 rs141249542 C T 3395581
chr13 111184492 rs111928873 T C 3395582
chr13 111184495 rs2479430 C A 3395583
chr13 111184496 rs186148890 C T 3395584
chr13 111184546 rs77071560 G A 3395585
chr13 111184901 rs531063845 A G 3395586
chr13 111184954 rs394559 C T 3395587
chr13 111184974 rs77968088 T C 3395588
chr13 111185016 rs6492282 G A 3395589
chr13 111185023 rs397697740 C CTATTT 3395590
chr13 111185023 rs60213123 C CTATTT 3395591
chr13 111185068 rs537332352 C A,G 3395592
chr13 111185182 rs570539918 C T 3395593
chr13 111185267 rs4771689 A G 3395594
chr13 111185327 rs115366524 G A 3395595
chr13 111185381 rs145679219 CT C 3395596
chr13 111185474 rs143982864 C T 3395597
chr13 111185507 rs147338198 G A 3395598
chr13 111185556 rs139325033 G C 3395599
chr13 111185674 rs11619434 G A 3395600
chr13 111185709 rs9559838 A T 3395601
chr13 111185742 rs142715730 C T 3395602
chr13 111185767 rs74596246 T C 3395603
chr13 111185771 rs575289103 T G 3395604
chr13 111185866 rs5806863 CA C 3395605
chr13 111185879 rs183227775 A T 3395606
chr13 111185950 rs188104805 G A 3395607
chr13 111185984 rs998489 G T 3395608
chr13 111185987 rs112495792 T A 3395609
chr13 111186009 rs114830124 G A 3395610
chr13 111186015 rs149907779 C G 3395611
chr13 111186030 rs1122092 T C 3395612
chr13 111186053 rs56663276 T A 3395613
chr13 111186065 rs5806864 T TC 3395614
chr13 111186140 rs536346801 T C 3395615
chr13 111186260 rs58682785 C T 3395616
chr13 111186295 rs534444935 TC T 3395617
chr13 111186300 rs59098701 C G 3395618
chr13 111186334 rs75454410 C T 3395619
chr13 111186337 rs58927807 T C 3395620
chr13 111186359 rs143948119 C T 3395621
chr13 111186369 rs77624870 A G 3395622
chr13 111186460 rs76432306 T C 3395623
chr13 111186485 rs9521821 A T 3395624
chr13 111186598 rs116716922 C A 3395625
chr13 111186614 rs568955339 A G 3395626
chr13 111186628 rs148677421 G A 3395627
chr13 111186638 rs9521822 C A 3395628
chr13 111186641 rs79775191 G A 3395629
chr13 111186795 rs143355319 C T 3395630
chr13 111186796 rs375725558 G A 3395631
chr13 111187007 rs187731730 C T 3395632
chr13 111187141 rs146766485 T C 3395633
chr13 111187181 rs11616542 T C 3395634
chr13 111187283 rs11619777 C A,T 3395635
chr13 111187343 rs185112104 G C 3395636
chr13 111187349 rs151249275 T G 3395637
chr13 111187361 rs66489837 AG A 3395638
chr13 111187374 rs573082743 TCTCA T 3395639
chr13 111187377 rs112220674 C T 3395640
chr13 111187432 rs1467650 T C 3395641
chr13 111187471 rs1467651 A G 3395642
chr13 111187473 rs117457856 G A 3395643
chr13 111187492 rs373986615 T C 3395644
chr13 111187657 rs80065874 G A 3395645
chr13 111187703 rs111503856 G A 3395646
chr13 111187750 rs1467652 G A 3395647
chr13 111187807 rs116317975 G A 3395648
chr13 111187818 rs188252751 C T 3395649
chr13 111187839 rs9515244 T A 3395650
chr13 111187913 rs142565936 C A 3395651
chr13 111187930 rs9652145 A C 3395652
chr13 111188011 rs184809454 C T 3395653
chr13 111188020 rs146728741 G A 3395654
chr13 111188044 rs74419499 C T 3395655
chr13 111188045 rs574503320 G A 3395656
chr13 111188065 rs115198839 G A 3395657
chr13 111188071 rs9652146 G A 3395658
chr13 111188087 rs9515245 T C 3395659
chr13 111188088 rs9515246 G A 3395660
chr13 111188135 rs9652147 A G 3395661
chr13 111188144 rs9515247 G A 3395662
chr13 111188183 rs9559839 C T 3395663
chr13 111188313 rs143336112 A G 3395664
chr13 111188377 rs144813804 C T 3395665
chr13 111188385 rs115655865 A C 3395666
chr13 111188399 rs537550587 T C 3395667
chr13 111188413 rs555936445 G A 3395668
chr13 111188420 rs116173496 G A 3395669
chr13 111188430 rs553810212 G C 3395670
chr13 111188482 rs564484547 G A 3395671
chr13 111188496 rs576561712 A G 3395672
chr13 111188520 rs9559840 G A 3395673
chr13 111188544 rs452294 C G 3395674
chr13 111188577 rs422183 T C 3395675
chr13 111188613 rs150544098 T C 3395676
chr13 111188642 rs549493389 C T 3395677
chr13 111188658 rs116715566 T A,C 3395678
chr13 111188728 rs7339017 C T 3395679
chr13 111188748 rs572197480 G A 3395680
Genes possibly regulated by ZNF274[chr13:111183656-111188794]
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Details of Genes
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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 to TFBS id More
Expression level of Genes
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No results
miRNAs possibly regulated by ZNF274[chr13:111183656-111188794]
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Details of miRNAs
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
Expression level of miRNAs
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No results