Variant report

Variant	rs4121366
Chromosome Location	chr11:102570760-102570761
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10791590	0.98[ASN][1000 genomes]
rs1276257	0.91[ASN][1000 genomes]
rs1276274	0.98[ASN][1000 genomes]
rs1276275	0.98[ASN][1000 genomes]
rs1276278	0.83[ASN][1000 genomes]
rs1276286	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1276287	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1276288	1.00[ASN][1000 genomes]
rs1276289	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1296594	0.98[ASN][1000 genomes]
rs1298740	0.98[ASN][1000 genomes]
rs1940041	0.85[ASN][1000 genomes]
rs1940473	0.96[ASN][1000 genomes]
rs1940478	1.00[ASN][1000 genomes]
rs1940480	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2155554	1.00[ASN][1000 genomes]
rs2155555	0.97[ASN][1000 genomes]
rs2464362	1.00[ASN][1000 genomes]
rs2464363	0.98[ASN][1000 genomes]
rs2509029	0.84[ASN][1000 genomes]
rs2509243	1.00[ASN][1000 genomes]
rs2509245	1.00[ASN][1000 genomes]
rs2701963	1.00[ASN][1000 genomes]
rs2701991	0.91[ASN][1000 genomes]
rs2701992	0.98[ASN][1000 genomes]
rs2701993	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs2845674	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2846342	0.86[ASN][1000 genomes]
rs2846365	0.95[CHB][hapmap];0.91[ASN][1000 genomes]
rs2846701	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2846704	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs2846705	0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs2846711	0.84[ASN][1000 genomes]
rs2846715	0.86[ASN][1000 genomes]
rs2846723	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[ASN][1000 genomes]
rs2846724	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:102568800-102572000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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