Variant report
Variant | rs7177210 |
---|---|
Chromosome Location | chr15:29847838-29847839 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11073082 | 0.92[ASN][1000 genomes] |
rs11631257 | 0.93[ASN][1000 genomes] |
rs11631497 | 0.93[ASN][1000 genomes] |
rs11632460 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11634036 | 0.93[ASN][1000 genomes] |
rs11634151 | 0.89[ASN][1000 genomes] |
rs11634681 | 0.91[ASN][1000 genomes] |
rs11636627 | 0.89[ASN][1000 genomes] |
rs11636674 | 0.93[ASN][1000 genomes] |
rs11636716 | 0.93[ASN][1000 genomes] |
rs11636798 | 0.93[ASN][1000 genomes] |
rs11638211 | 0.93[ASN][1000 genomes] |
rs12913565 | 0.92[ASN][1000 genomes] |
rs12917374 | 0.93[ASN][1000 genomes] |
rs28643378 | 0.86[ASN][1000 genomes] |
rs34390915 | 0.92[ASN][1000 genomes] |
rs34747334 | 0.89[ASN][1000 genomes] |
rs34747429 | 0.89[ASN][1000 genomes] |
rs35031027 | 0.90[ASN][1000 genomes] |
rs35429322 | 0.84[ASN][1000 genomes] |
rs35506120 | 0.83[ASN][1000 genomes] |
rs35530312 | 0.84[ASN][1000 genomes] |
rs36004058 | 0.93[ASN][1000 genomes] |
rs56086218 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs56236273 | 0.90[EUR][1000 genomes] |
rs56268007 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs56306531 | 0.90[EUR][1000 genomes] |
rs58484246 | 0.86[EUR][1000 genomes] |
rs58919351 | 0.84[ASN][1000 genomes] |
rs59800030 | 0.85[EUR][1000 genomes] |
rs6495725 | 0.87[ASN][1000 genomes] |
rs66635026 | 0.89[ASN][1000 genomes] |
rs66870189 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs66912732 | 0.91[ASN][1000 genomes] |
rs66919218 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67149073 | 0.93[ASN][1000 genomes] |
rs67367754 | 0.85[ASN][1000 genomes] |
rs67542351 | 0.93[ASN][1000 genomes] |
rs67695074 | 0.93[ASN][1000 genomes] |
rs7162050 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7162550 | 0.88[ASN][1000 genomes] |
rs7162759 | 0.93[ASN][1000 genomes] |
rs7162953 | 0.92[ASN][1000 genomes] |
rs7163749 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7164745 | 0.93[ASN][1000 genomes] |
rs7166001 | 0.93[ASN][1000 genomes] |
rs7166045 | 0.93[ASN][1000 genomes] |
rs7167974 | 0.92[ASN][1000 genomes] |
rs7169924 | 0.93[ASN][1000 genomes] |
rs7169938 | 0.93[ASN][1000 genomes] |
rs7170313 | 0.93[ASN][1000 genomes] |
rs7170395 | 0.91[ASN][1000 genomes] |
rs7170509 | 0.91[ASN][1000 genomes] |
rs7170926 | 0.92[ASN][1000 genomes] |
rs7171420 | 0.88[ASN][1000 genomes] |
rs7171641 | 0.84[ASN][1000 genomes] |
rs7172391 | 0.93[ASN][1000 genomes] |
rs7174101 | 0.93[ASN][1000 genomes] |
rs7178072 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7179489 | 0.92[ASN][1000 genomes] |
rs7180209 | 0.92[ASN][1000 genomes] |
rs7181288 | 0.92[ASN][1000 genomes] |
rs7182730 | 0.93[ASN][1000 genomes] |
rs7182850 | 0.93[ASN][1000 genomes] |
rs7183007 | 0.93[ASN][1000 genomes] |
rs7494798 | 0.92[ASN][1000 genomes] |
rs7495240 | 0.93[ASN][1000 genomes] |
rs7495317 | 0.93[ASN][1000 genomes] |
rs7495389 | 0.93[ASN][1000 genomes] |
rs7497385 | 0.92[ASN][1000 genomes] |
rs7497443 | 0.93[ASN][1000 genomes] |
rs8024352 | 0.93[ASN][1000 genomes] |
rs8025341 | 0.93[ASN][1000 genomes] |
rs8028417 | 0.89[ASN][1000 genomes] |
rs8028448 | 0.89[ASN][1000 genomes] |
rs8028924 | 0.89[ASN][1000 genomes] |
rs8029633 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs8031657 | 0.93[ASN][1000 genomes] |
rs8032172 | 0.88[ASN][1000 genomes] |
rs8032779 | 0.93[ASN][1000 genomes] |
rs8033591 | 0.89[ASN][1000 genomes] |
rs8039813 | 0.93[ASN][1000 genomes] |
rs8040300 | 0.93[ASN][1000 genomes] |
rs8041925 | 0.91[ASN][1000 genomes] |
rs977060 | 0.88[ASN][1000 genomes] |
rs9806500 | 0.85[ASN][1000 genomes] |
rs9806691 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs982914 | 0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv456736 | chr15:29327352-30208654 | Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
2 | nsv568675 | chr15:29327352-30208654 | Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
3 | nsv903747 | chr15:29361126-30008977 | Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
4 | esv3364436 | chr15:29459739-29853229 | Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
5 | nsv995038 | chr15:29744279-30366124 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
6 | nsv832943 | chr15:29788334-29924284 | Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv456737 | chr15:29812777-29875999 | Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv568680 | chr15:29812777-29875999 | Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
9 | nsv456738 | chr15:29812777-29889806 | Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
10 | nsv1038495 | chr15:29825859-30351687 | Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
11 | nsv542293 | chr15:29825859-30351687 | Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:29842000-29849000 | Weak transcription | Pancreas | Pancrea |
2 | chr15:29843400-29848400 | Weak transcription | Fetal Lung | lung |
3 | chr15:29846400-29849200 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
4 | chr15:29847000-29848400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
5 | chr15:29847400-29848000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr15:29847800-29848200 | Enhancers | H1 Cell Line | embryonic stem cell |
7 | chr15:29847800-29848200 | Enhancers | H9 Cell Line | embryonic stem cell |
8 | chr15:29847800-29848200 | Enhancers | Lung | lung |
9 | chr15:29847800-29848600 | Bivalent Enhancer | H1 Derived Mesenchymal Stem Cells | ES cell derived |