Variant report

Variant	rs12774334
Chromosome Location	chr10:97567100-97567101
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11592809	0.84[AMR][1000 genomes]
rs11592937	0.84[EUR][1000 genomes]
rs11593038	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11593693	0.81[AMR][1000 genomes]
rs11594340	0.90[EUR][1000 genomes]
rs11595122	0.86[EUR][1000 genomes]
rs11595248	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11598540	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12761112	0.81[AMR][1000 genomes]
rs12761960	0.84[EUR][1000 genomes]
rs12763743	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12767650	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12770313	0.86[EUR][1000 genomes]
rs12770849	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12775780	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12779833	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12780375	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12781327	0.81[AMR][1000 genomes]
rs12782273	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1409710	0.84[AMR][1000 genomes]
rs2275272	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2296690	0.84[AMR][1000 genomes]
rs3176886	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3176888	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3181115	0.85[EUR][1000 genomes]
rs34296389	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34533159	0.81[AMR][1000 genomes]
rs34630379	0.84[EUR][1000 genomes]
rs34832675	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34833309	0.84[EUR][1000 genomes]
rs34836127	0.84[EUR][1000 genomes]
rs35700869	0.88[EUR][1000 genomes]
rs35712039	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35987262	0.82[EUR][1000 genomes]
rs3793751	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs55859130	0.90[ASN][1000 genomes]
rs56853511	1.00[ASN][1000 genomes]
rs58636501	0.90[ASN][1000 genomes]
rs68078796	0.88[EUR][1000 genomes]
rs71482374	0.86[EUR][1000 genomes]
rs71482376	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71482377	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71482378	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531923	chr10:97366055-97725757	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv895905	chr10:97513362-97686064	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv895906	chr10:97513362-97703650	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv895907	chr10:97529318-97686064	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv895908	chr10:97544513-97724247	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97553000-97576200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:97558800-97570600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr10:97566200-97567800	Enhancers	Primary B cells from peripheral blood	blood
4	chr10:97566400-97567400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr10:97566600-97567200	Flanking Active TSS	HepG2	liver
6	chr10:97566800-97567200	Enhancers	Spleen	Spleen
7	chr10:97566800-97568600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr10:97567000-97567200	Enhancers	Primary B cells from cord blood	blood
9	chr10:97567000-97568600	ZNF genes & repeats	GM12878-XiMat	blood
10	chr10:97567000-97569200	Weak transcription	Primary monocytes fromperipheralblood	blood

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