Variant report

Variant	rs594122
Chromosome Location	chr11:84807684-84807685
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10898360	0.81[ASN][1000 genomes]
rs10898364	0.86[ASN][1000 genomes]
rs1227842	0.86[EUR][1000 genomes]
rs1227843	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1238728	0.86[EUR][1000 genomes]
rs12792714	0.83[EUR][1000 genomes]
rs1823777	0.84[ASN][1000 genomes]
rs2252376	0.85[EUR][1000 genomes]
rs2444254	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2453151	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2509053	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2513242	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs527389	0.88[EUR][1000 genomes]
rs540153	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs542892	0.88[EUR][1000 genomes]
rs543740	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs555156	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs555259	0.83[EUR][1000 genomes]
rs560214	0.85[EUR][1000 genomes]
rs560587	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs567594	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs568330	0.85[EUR][1000 genomes]
rs568641	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs573650	0.90[EUR][1000 genomes]
rs581943	0.81[EUR][1000 genomes]
rs592166	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs593800	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs595435	0.85[EUR][1000 genomes]
rs605652	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs614689	0.83[ASN][1000 genomes]
rs617231	0.87[EUR][1000 genomes]
rs626013	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs626531	0.84[EUR][1000 genomes]
rs631370	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs632351	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs633562	0.86[EUR][1000 genomes]
rs650374	0.90[EUR][1000 genomes]
rs652830	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs658749	0.83[EUR][1000 genomes]
rs660274	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs666735	0.87[ASN][1000 genomes]
rs675160	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs675217	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs685294	0.88[EUR][1000 genomes]
rs694142	0.88[EUR][1000 genomes]
rs7110248	0.81[ASN][1000 genomes]
rs7126522	0.81[ASN][1000 genomes]
rs7127990	0.85[EUR][1000 genomes]
rs7948646	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	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
3	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
4	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
5	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
6	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
7	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84807600-84809000	Enhancers	Primary B cells from peripheral blood	blood

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