Variant report
Variant | rs10829302 |
---|---|
Chromosome Location | chr10:27945256-27945257 |
allele | C/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 |
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rs_ID | r2[population] |
---|---|
rs1002861 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1027342 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10508722 | 1.00[EUR][1000 genomes] |
rs10508724 | 0.86[EUR][1000 genomes] |
rs10764699 | 0.86[EUR][1000 genomes] |
rs10764718 | 1.00[EUR][1000 genomes] |
rs10764719 | 1.00[EUR][1000 genomes] |
rs10826346 | 0.86[EUR][1000 genomes] |
rs10829285 | 1.00[EUR][1000 genomes] |
rs10829286 | 1.00[EUR][1000 genomes] |
rs10829294 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10829296 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10829304 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10829305 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11006697 | 1.00[EUR][1000 genomes] |
rs11006698 | 1.00[EUR][1000 genomes] |
rs11006699 | 1.00[EUR][1000 genomes] |
rs11006700 | 1.00[EUR][1000 genomes] |
rs11015826 | 0.86[EUR][1000 genomes] |
rs11015832 | 0.86[EUR][1000 genomes] |
rs11015833 | 0.86[EUR][1000 genomes] |
rs11015836 | 0.83[EUR][1000 genomes] |
rs11015840 | 0.86[EUR][1000 genomes] |
rs11015856 | 0.86[EUR][1000 genomes] |
rs11015857 | 0.86[EUR][1000 genomes] |
rs11015858 | 0.86[EUR][1000 genomes] |
rs11015875 | 0.86[EUR][1000 genomes] |
rs11015898 | 1.00[EUR][1000 genomes] |
rs11015923 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11015927 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11015928 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11015935 | 0.98[ASN][1000 genomes] |
rs11015936 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11015938 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11015942 | 0.82[AMR][1000 genomes] |
rs11015946 | 1.00[EUR][1000 genomes] |
rs11015948 | 1.00[EUR][1000 genomes] |
rs11015957 | 1.00[EUR][1000 genomes] |
rs11015958 | 0.86[EUR][1000 genomes] |
rs11015969 | 1.00[EUR][1000 genomes] |
rs11015973 | 1.00[EUR][1000 genomes] |
rs11015980 | 1.00[EUR][1000 genomes] |
rs11015981 | 1.00[EUR][1000 genomes] |
rs12217955 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12218027 | 1.00[EUR][1000 genomes] |
rs12218420 | 0.86[EUR][1000 genomes] |
rs12219258 | 0.86[EUR][1000 genomes] |
rs12219316 | 0.96[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12219955 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12220217 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12220463 | 0.86[EUR][1000 genomes] |
rs12257550 | 0.86[EUR][1000 genomes] |
rs12264856 | 1.00[EUR][1000 genomes] |
rs12411785 | 0.91[AMR][1000 genomes] |
rs12411792 | 0.91[AMR][1000 genomes] |
rs12411804 | 0.86[EUR][1000 genomes] |
rs12412077 | 0.86[AMR][1000 genomes] |
rs12569521 | 1.00[EUR][1000 genomes] |
rs12571836 | 0.86[EUR][1000 genomes] |
rs12572531 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1690678 | 0.95[ASN][1000 genomes] |
rs1690690 | 0.80[ASN][1000 genomes] |
rs17756134 | 0.86[EUR][1000 genomes] |
rs17756253 | 0.86[EUR][1000 genomes] |
rs1907388 | 0.86[EUR][1000 genomes] |
rs2242356 | 0.86[EUR][1000 genomes] |
rs57812861 | 1.00[EUR][1000 genomes] |
rs72629759 | 0.86[EUR][1000 genomes] |
rs72629760 | 0.86[EUR][1000 genomes] |
rs72629761 | 0.86[EUR][1000 genomes] |
rs72629762 | 0.86[EUR][1000 genomes] |
rs72629763 | 0.86[EUR][1000 genomes] |
rs72629764 | 0.86[EUR][1000 genomes] |
rs72629766 | 1.00[EUR][1000 genomes] |
rs72629767 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs72629772 | 1.00[EUR][1000 genomes] |
rs72629774 | 1.00[EUR][1000 genomes] |
rs72629775 | 1.00[EUR][1000 genomes] |
rs72629776 | 1.00[EUR][1000 genomes] |
rs72629777 | 1.00[EUR][1000 genomes] |
rs72629778 | 1.00[EUR][1000 genomes] |
rs72631837 | 1.00[EUR][1000 genomes] |
rs72631838 | 1.00[EUR][1000 genomes] |
rs72631839 | 1.00[EUR][1000 genomes] |
rs7358151 | 0.86[EUR][1000 genomes] |
rs8181307 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv550241 | chr10:27569521-28025771 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
2 | esv3368825 | chr10:27864181-28043820 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
3 | nsv894985 | chr10:27869503-27957785 | Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv894986 | chr10:27904646-27957785 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv3376883 | chr10:27945120-27945279 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:27933800-27963600 | Weak transcription | Ovary | ovary |
2 | chr10:27941600-27963600 | Weak transcription | Stomach Smooth Muscle | stomach |
3 | chr10:27944400-27947000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
4 | chr10:27944400-27948600 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
5 | chr10:27944600-27947800 | Weak transcription | NHDF-Ad | bronchial |
6 | chr10:27945000-27945400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
7 | chr10:27945000-27947200 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
8 | chr10:27945200-27946000 | Enhancers | Monocytes-CD14+_RO01746 | blood |