Variant report

Variant	rs11233815
Chromosome Location	chr11:83645487-83645488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10898182	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[ASN][1000 genomes]
rs10898183	0.96[ASN][1000 genomes]
rs10898184	0.97[ASN][1000 genomes]
rs10898185	1.00[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs11233817	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[ASN][1000 genomes]
rs11233818	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233819	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233820	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233821	1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233822	0.85[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233823	0.97[ASN][1000 genomes]
rs11233824	0.97[ASN][1000 genomes]
rs11233827	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233830	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11233831	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233832	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233837	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11233842	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12222190	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12225678	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12278503	0.82[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs1319736	1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs1384753	1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[ASN][1000 genomes]
rs790366	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv555608	chr11:83633189-83651102	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83629800-83661800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr11:83634600-83649400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr11:83639400-83649600	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:83639600-83659400	Weak transcription	Ovary	ovary
5	chr11:83644000-83645600	Enhancers	Brain Germinal Matrix	brain

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