Variant report
Variant | rs13358459 |
---|---|
Chromosome Location | chr5:41902191-41902192 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000172262 | Chromatin interaction |
ENSG00000248668 | Chromatin interaction |
ENSG00000083720 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10035434 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10040757 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10043326 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10043371 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10044526 | 0.88[AMR][1000 genomes] |
rs10045473 | 1.00[EUR][1000 genomes] |
rs10051322 | 1.00[EUR][1000 genomes] |
rs10052226 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10053522 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10054130 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10057546 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10057587 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10057645 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10059424 | 0.97[EUR][1000 genomes] |
rs10060170 | 1.00[EUR][1000 genomes] |
rs10062703 | 1.00[EUR][1000 genomes] |
rs10064298 | 1.00[EUR][1000 genomes] |
rs10064380 | 0.87[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs10065016 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10065335 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10069638 | 1.00[EUR][1000 genomes] |
rs10070201 | 1.00[EUR][1000 genomes] |
rs10075429 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10076689 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10077481 | 0.95[EUR][1000 genomes] |
rs10078011 | 0.95[EUR][1000 genomes] |
rs10079651 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1027348 | 0.95[EUR][1000 genomes] |
rs10472357 | 1.00[EUR][1000 genomes] |
rs10472359 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs10473252 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10473255 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11738449 | 0.82[AMR][1000 genomes] |
rs11738956 | 0.95[EUR][1000 genomes] |
rs11742939 | 0.82[AMR][1000 genomes] |
rs11745460 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11745530 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11746530 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11747648 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11748933 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13355194 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13357951 | 1.00[EUR][1000 genomes] |
rs13360765 | 0.88[AMR][1000 genomes] |
rs1567323 | 1.00[EUR][1000 genomes] |
rs16872052 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16872094 | 0.85[AMR][1000 genomes] |
rs16872097 | 0.88[AMR][1000 genomes] |
rs16872100 | 0.82[AMR][1000 genomes] |
rs170299 | 0.87[EUR][1000 genomes] |
rs17339188 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1813615 | 0.82[AMR][1000 genomes] |
rs1813616 | 0.82[AMR][1000 genomes] |
rs2011105 | 0.82[AMR][1000 genomes] |
rs2113053 | 0.83[EUR][1000 genomes] |
rs2231910 | 1.00[EUR][1000 genomes] |
rs28647448 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs316746 | 0.87[EUR][1000 genomes] |
rs316747 | 0.87[EUR][1000 genomes] |
rs316748 | 0.87[EUR][1000 genomes] |
rs316749 | 0.87[EUR][1000 genomes] |
rs316750 | 0.87[EUR][1000 genomes] |
rs316752 | 0.87[EUR][1000 genomes] |
rs316754 | 0.87[EUR][1000 genomes] |
rs316756 | 0.87[EUR][1000 genomes] |
rs316757 | 0.87[EUR][1000 genomes] |
rs316758 | 0.87[EUR][1000 genomes] |
rs34493032 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs35890705 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4957178 | 1.00[EUR][1000 genomes] |
rs4957180 | 1.00[EUR][1000 genomes] |
rs4957436 | 0.94[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs4957437 | 1.00[EUR][1000 genomes] |
rs4957438 | 1.00[EUR][1000 genomes] |
rs57944767 | 0.90[EUR][1000 genomes] |
rs582920 | 0.92[EUR][1000 genomes] |
rs583090 | 0.87[EUR][1000 genomes] |
rs584067 | 0.90[EUR][1000 genomes] |
rs590851 | 0.90[EUR][1000 genomes] |
rs591384 | 0.85[EUR][1000 genomes] |
rs602274 | 0.90[EUR][1000 genomes] |
rs607620 | 0.87[EUR][1000 genomes] |
rs61058110 | 0.95[EUR][1000 genomes] |
rs621944 | 0.87[EUR][1000 genomes] |
rs627476 | 0.87[EUR][1000 genomes] |
rs641270 | 0.87[EUR][1000 genomes] |
rs654400 | 0.87[EUR][1000 genomes] |
rs67152480 | 0.95[EUR][1000 genomes] |
rs678061 | 0.92[EUR][1000 genomes] |
rs72746926 | 0.95[EUR][1000 genomes] |
rs72746928 | 0.95[EUR][1000 genomes] |
rs72746930 | 0.95[EUR][1000 genomes] |
rs72746932 | 0.95[EUR][1000 genomes] |
rs72746933 | 0.93[EUR][1000 genomes] |
rs72746952 | 0.95[EUR][1000 genomes] |
rs72746962 | 0.90[EUR][1000 genomes] |
rs72746966 | 0.95[EUR][1000 genomes] |
rs72746968 | 0.95[EUR][1000 genomes] |
rs72746975 | 0.95[EUR][1000 genomes] |
rs72746983 | 0.95[EUR][1000 genomes] |
rs72746985 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72746995 | 1.00[EUR][1000 genomes] |
rs72746996 | 0.92[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs72746997 | 0.95[EUR][1000 genomes] |
rs72746999 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72747000 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72747001 | 1.00[EUR][1000 genomes] |
rs72747002 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748607 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748608 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748609 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748611 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748613 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748614 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748616 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748619 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748620 | 1.00[EUR][1000 genomes] |
rs72748623 | 0.83[EUR][1000 genomes] |
rs72748635 | 0.85[AMR][1000 genomes] |
rs72748641 | 0.82[AMR][1000 genomes] |
rs72761834 | 0.87[EUR][1000 genomes] |
rs7341062 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7712106 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7723992 | 1.00[EUR][1000 genomes] |
rs9292826 | 0.95[EUR][1000 genomes] |
rs9292828 | 0.95[EUR][1000 genomes] |
rs9292832 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9885033 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9885117 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs989747 | 0.82[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2762518 | chr5:41780210-41935113 | Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 108 gene(s) | inside rSNPs | diseases |
2 | nsv830272 | chr5:41833365-41986167 | Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 111 gene(s) | inside rSNPs | diseases |
3 | nsv830273 | chr5:41867296-42066070 | Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 111 gene(s) | inside rSNPs | diseases |
4 | nsv933208 | chr5:41879946-42876624 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 112 gene(s) | inside rSNPs | diseases |
5 | esv3508785 | chr5:41900095-41904893 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
6 | nsv327668 | chr5:41901383-41909830 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
7 | esv3469161 | chr5:41901765-41903841 | Active TSS Flanking Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
8 | esv3508784 | chr5:41901813-41903820 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
9 | esv3469160 | chr5:41901819-41903820 | Active TSS Flanking Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
10 | esv3469164 | chr5:41901829-41903802 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
11 | esv3508788 | chr5:41901833-41903785 | Active TSS Enhancers Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
12 | esv3469162 | chr5:41901853-41903778 | Active TSS Enhancers Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
13 | esv3508789 | chr5:41901860-41903770 | Enhancers Flanking Active TSS Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
14 | esv13889 | chr5:41901871-41903659 | Enhancers Active TSS Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 12 gene(s) | inside rSNPs | diseases |
15 | esv3469159 | chr5:41901905-41903722 | Flanking Active TSS Enhancers Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
16 | esv3508787 | chr5:41901915-41903724 | Active TSS Flanking Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
17 | esv3469165 | chr5:41901920-41903719 | Active TSS Enhancers Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 14 gene(s) | inside rSNPs | diseases |
18 | esv3508790 | chr5:41901920-41903719 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 14 gene(s) | inside rSNPs | diseases |
19 | nsv597881 | chr5:41901966-41903583 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 11 gene(s) | inside rSNPs | diseases |
20 | nsv492147 | chr5:41902086-42896162 | Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 113 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:41899600-41903200 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr5:41900000-41903800 | Weak transcription | Gastric | stomach |
3 | chr5:41900400-41903600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |