Variant report

Variant	rs186341
Chromosome Location	chr8:90655962-90655963
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11986477	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11987361	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11997127	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160421	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160425	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160426	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160428	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160431	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160432	0.88[ASN][1000 genomes]
rs160433	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160434	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160436	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160442	0.89[EUR][1000 genomes]
rs160443	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160452	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160454	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs160455	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs184309	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs216991	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2338843	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs410394	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57897527	0.89[EUR][1000 genomes]
rs58916408	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60246734	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61458082	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73289972	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73289974	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73291834	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73291835	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73291867	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73304818	0.89[EUR][1000 genomes]
rs7840849	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv870380	chr8:90546585-90720182	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1028026	chr8:90553930-90678631	Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv982109	chr8:90556188-90703631	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1026523	chr8:90558935-90722580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv831389	chr8:90575517-90753120	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv1017263	chr8:90605445-90722580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90629400-90659000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90643600-90659600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:90646800-90658200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:90654600-90656400	Weak transcription	Lung	lung
5	chr8:90655200-90656000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:90655400-90662800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:90655600-90656000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:90655600-90656200	Enhancers	Fetal Heart	heart
9	chr8:90655800-90656200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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