Variant report

Variant	rs694142
Chromosome Location	chr11:84741052-84741053
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10792792	0.96[CEU][hapmap]
rs10792794	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10898336	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10898343	0.96[CEU][hapmap]
rs1227842	0.85[CEU][hapmap]
rs1227843	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1237921	0.94[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs1238728	0.85[CEU][hapmap]
rs1940122	0.96[CEU][hapmap]
rs1940123	0.96[CEU][hapmap]
rs1940133	0.96[CEU][hapmap]
rs2155410	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2155411	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs2155412	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs2252376	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2253167	0.96[CEU][hapmap]
rs2444254	0.96[CEU][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2444255	0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2453151	0.85[CEU][hapmap]
rs2509053	0.96[CEU][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2509056	0.88[CEU][hapmap]
rs3862779	0.96[CEU][hapmap]
rs490286	0.81[CEU][hapmap]
rs527389	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs542892	0.88[CEU][hapmap]
rs543740	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs555156	0.84[CEU][hapmap]
rs555259	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs560214	0.84[CEU][hapmap]
rs560587	0.87[EUR][1000 genomes]
rs567594	0.92[CEU][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs568641	0.88[CEU][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs573650	0.90[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs574671	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs575189	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs577950	0.96[CEU][hapmap]
rs578782	0.85[CEU][hapmap]
rs581943	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs582884	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs589093	0.81[CEU][hapmap]
rs592166	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs592622	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs593800	0.85[CEU][hapmap]
rs594122	0.88[EUR][1000 genomes]
rs595435	0.84[CEU][hapmap]
rs596556	0.96[CEU][hapmap]
rs597592	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs601375	0.88[CEU][hapmap]
rs605652	0.90[CEU][hapmap]
rs607864	0.85[CEU][hapmap]
rs613265	0.92[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs613315	0.88[CEU][hapmap]
rs617231	0.88[CEU][hapmap]
rs621007	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs625495	0.96[CEU][hapmap]
rs626531	0.89[CEU][hapmap]
rs626700	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs630948	0.89[CEU][hapmap]
rs631370	0.80[CEU][hapmap]
rs632351	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs635032	0.96[CEU][hapmap]
rs641655	0.84[CEU][hapmap]
rs641958	0.96[CEU][hapmap]
rs643891	0.96[CEU][hapmap]
rs646324	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs646502	0.88[CEU][hapmap]
rs648506	0.82[EUR][1000 genomes]
rs649468	0.92[CEU][hapmap]
rs650374	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs651661	0.96[CEU][hapmap]
rs652830	0.89[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs658749	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6592215	0.96[CEU][hapmap]
rs6592216	0.96[CEU][hapmap]
rs6592220	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6592221	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6592222	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs660274	0.85[CEU][hapmap]
rs666735	0.81[CEU][hapmap]
rs670998	0.96[CEU][hapmap]
rs675160	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs675217	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs675255	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs679745	0.80[CEU][hapmap]
rs685294	0.92[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs686009	0.85[CEU][hapmap]
rs687695	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs688329	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs689226	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs7127990	0.96[CEU][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1048051	chr11:84419442-84784233	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541109	chr11:84419442-84784233	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv430415	chr11:84661652-84833852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1055097	chr11:84672444-84810441	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv555629	chr11:84720020-84744926	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84740800-84741600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:84740800-84741800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr11:84741000-84741600	Enhancers	A549	lung

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