Variant report
Variant | rs8029393 |
---|---|
Chromosome Location | chr15:35415521-35415522 |
allele | G/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] |
---|---|
rs12324560 | 1.00[EUR][1000 genomes] |
rs12324696 | 1.00[EUR][1000 genomes] |
rs6495734 | 1.00[EUR][1000 genomes] |
rs6495735 | 1.00[EUR][1000 genomes] |
rs6495737 | 1.00[EUR][1000 genomes] |
rs6495740 | 1.00[EUR][1000 genomes] |
rs6495741 | 1.00[EUR][1000 genomes] |
rs7165876 | 1.00[EUR][1000 genomes] |
rs7166694 | 1.00[ASN][1000 genomes] |
rs7174153 | 1.00[EUR][1000 genomes] |
rs7177151 | 1.00[EUR][1000 genomes] |
rs7182812 | 1.00[EUR][1000 genomes] |
rs7183352 | 1.00[EUR][1000 genomes] |
rs72704759 | 1.00[EUR][1000 genomes] |
rs72704763 | 1.00[EUR][1000 genomes] |
rs72704771 | 1.00[EUR][1000 genomes] |
rs72704774 | 1.00[EUR][1000 genomes] |
rs72704775 | 1.00[EUR][1000 genomes] |
rs72704778 | 1.00[EUR][1000 genomes] |
rs72704781 | 1.00[EUR][1000 genomes] |
rs72705008 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705010 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705011 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705012 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705016 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705020 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705023 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705027 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72705033 | 1.00[EUR][1000 genomes] |
rs72705035 | 1.00[EUR][1000 genomes] |
rs72705094 | 1.00[EUR][1000 genomes] |
rs72705099 | 1.00[EUR][1000 genomes] |
rs72707010 | 1.00[EUR][1000 genomes] |
rs72707025 | 1.00[EUR][1000 genomes] |
rs72707037 | 1.00[EUR][1000 genomes] |
rs72707049 | 1.00[EUR][1000 genomes] |
rs72707050 | 1.00[EUR][1000 genomes] |
rs72707054 | 1.00[EUR][1000 genomes] |
rs72707055 | 1.00[EUR][1000 genomes] |
rs72707056 | 1.00[EUR][1000 genomes] |
rs72707059 | 1.00[EUR][1000 genomes] |
rs72707060 | 1.00[EUR][1000 genomes] |
rs72707062 | 1.00[EUR][1000 genomes] |
rs72707066 | 1.00[EUR][1000 genomes] |
rs72707067 | 1.00[EUR][1000 genomes] |
rs72707071 | 1.00[EUR][1000 genomes] |
rs72707072 | 1.00[EUR][1000 genomes] |
rs8025416 | 1.00[EUR][1000 genomes] |
rs8026023 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs8028485 | 1.00[EUR][1000 genomes] |
rs8031014 | 1.00[EUR][1000 genomes] |
rs9806356 | 1.00[EUR][1000 genomes] |
rs9806378 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3350109 | chr15:34668106-35534229 | Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
2 | nsv522411 | chr15:34953986-35462981 | Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
3 | nsv1052721 | chr15:35381487-35437841 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
4 | nsv976920 | chr15:35413394-35416762 | Weak transcription Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:35407600-35415600 | Weak transcription | Pancreas | Pancrea |
2 | chr15:35413200-35419400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
3 | chr15:35414000-35431000 | Weak transcription | Aorta | Aorta |
4 | chr15:35414200-35416800 | Weak transcription | Fetal Stomach | stomach |