Variant report

Variant	rs6592166
Chromosome Location	chr11:83863711-83863712
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1014066	0.82[ASN][1000 genomes]
rs10501555	0.82[ASN][1000 genomes]
rs10736760	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10751104	0.82[EUR][1000 genomes]
rs10792720	0.83[EUR][1000 genomes]
rs10792721	0.81[EUR][1000 genomes]
rs10792722	0.83[EUR][1000 genomes]
rs10792723	0.81[EUR][1000 genomes]
rs10792724	0.81[ASN][1000 genomes]
rs10792725	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10792726	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10898205	0.83[EUR][1000 genomes]
rs10898206	0.83[EUR][1000 genomes]
rs10898207	0.83[EUR][1000 genomes]
rs1377745	0.85[ASN][1000 genomes]
rs1454018	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1454019	0.85[ASN][1000 genomes]
rs1551334	0.83[EUR][1000 genomes]
rs1620817	0.89[ASN][1000 genomes]
rs1670679	0.89[ASN][1000 genomes]
rs1894169	0.81[EUR][1000 genomes]
rs1945808	0.83[EUR][1000 genomes]
rs1945819	0.83[ASN][1000 genomes]
rs1945820	0.82[ASN][1000 genomes]
rs1945821	0.82[ASN][1000 genomes]
rs1945822	0.81[ASN][1000 genomes]
rs1945823	0.81[ASN][1000 genomes]
rs1945824	0.81[ASN][1000 genomes]
rs1945825	0.82[ASN][1000 genomes]
rs1945826	0.81[ASN][1000 genomes]
rs1945827	0.83[EUR][1000 genomes]
rs2000961	0.85[ASN][1000 genomes]
rs6592165	0.81[EUR][1000 genomes]
rs7104249	0.83[EUR][1000 genomes]
rs7123516	0.81[EUR][1000 genomes]
rs7123584	0.81[EUR][1000 genomes]
rs756196	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs756197	0.82[ASN][1000 genomes]
rs7925643	0.83[EUR][1000 genomes]
rs7948263	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs872510	0.82[ASN][1000 genomes]
rs872511	0.82[ASN][1000 genomes]
rs872512	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs884873	0.81[ASN][1000 genomes]
rs9787893	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1051279	chr11:83818647-83872815	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83858400-83867200	Weak transcription	Brain Inferior Temporal Lobe	brain

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