Variant report

Variant	rs11188488
Chromosome Location	chr10:97559527-97559528
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10159941	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10509687	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs10748634	0.84[CHB][hapmap]
rs10748635	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs10748637	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10748638	0.86[CHB][hapmap]
rs10786230	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs10786235	1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs10786238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882646	0.83[CHB][hapmap]
rs10882653	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs10882664	0.92[CHB][hapmap]
rs10882665	0.92[CHB][hapmap]
rs10882670	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs11188441	0.82[ASN][1000 genomes]
rs11188459	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs11188470	0.81[ASN][1000 genomes]
rs11188482	0.88[ASN][1000 genomes]
rs11188485	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11498722	0.80[ASN][1000 genomes]
rs11528098	0.90[ASN][1000 genomes]
rs11819621	1.00[CEU][hapmap]
rs11819652	1.00[CEU][hapmap]
rs12240959	0.90[ASN][1000 genomes]
rs12262943	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1340837	0.86[JPT][hapmap]
rs1342791	0.92[CHB][hapmap]
rs17111041	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs17111249	1.00[CEU][hapmap]
rs1933166	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs1933169	0.92[CHB][hapmap]
rs1953710	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs2211002	0.84[CHB][hapmap]
rs2225893	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs2861149	0.86[CHB][hapmap]
rs2901873	0.92[CHB][hapmap]
rs2901874	0.85[ASN][1000 genomes]
rs2901895	1.00[CEU][hapmap]
rs3176883	1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs3181123	0.92[CHB][hapmap]
rs3793748	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs3949478	0.92[CHB][hapmap]
rs4075311	0.85[JPT][hapmap]
rs4290159	0.82[CHB][hapmap]
rs4409759	0.88[ASN][1000 genomes]
rs4457685	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs4501930	0.92[CHB][hapmap]
rs4918950	0.84[CHB][hapmap]
rs4918964	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs496426	0.84[CHB][hapmap]
rs497331	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.81[AFR][1000 genomes]
rs60227189	0.88[ASN][1000 genomes]
rs6584026	1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs6584028	1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs6584031	0.90[ASN][1000 genomes]
rs6584033	1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs7069234	1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs7073723	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7081414	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7084741	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7085059	0.82[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs7085594	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7090320	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7098750	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs7100137	0.97[ASN][1000 genomes]
rs7901116	0.85[ASN][1000 genomes]
rs7902190	1.00[CHB][hapmap]
rs7905653	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs7907476	1.00[CEU][hapmap]
rs7909569	0.83[CHB][hapmap]
rs7915345	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7920850	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs945958	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv1052213	chr10:97536795-97561941	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97553000-97576200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:97556800-97560400	Weak transcription	Primary B cells from cord blood	blood
3	chr10:97557200-97560000	ZNF genes & repeats	GM12878-XiMat	blood
4	chr10:97558800-97566200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr10:97558800-97566400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:97558800-97570600	Weak transcription	Monocytes-CD14+_RO01746	blood

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