Variant report

Variant	rs11116995
Chromosome Location	chr12:86105320-86105321
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10779199	0.97[EUR][1000 genomes]
rs10863053	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10863064	0.95[EUR][1000 genomes]
rs11116993	0.81[AFR][1000 genomes]
rs11117012	0.95[EUR][1000 genomes]
rs12316200	0.81[AFR][1000 genomes]
rs12316964	0.89[AFR][1000 genomes]
rs12319540	0.81[AFR][1000 genomes]
rs17322447	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3041468	0.96[EUR][1000 genomes]
rs4897820	0.96[EUR][1000 genomes]
rs4897833	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56092643	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61928654	0.97[EUR][1000 genomes]
rs61928655	0.97[EUR][1000 genomes]
rs61928658	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61928659	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928922	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61928923	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61928924	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928925	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928926	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928927	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928930	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61928931	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61928936	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61928938	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61928939	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61929961	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61930083	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930090	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930091	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7132191	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7296027	0.97[EUR][1000 genomes]
rs7298784	0.97[EUR][1000 genomes]
rs7299727	0.97[EUR][1000 genomes]
rs7316003	0.89[AFR][1000 genomes]
rs7969224	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7972166	0.89[AFR][1000 genomes]
rs958414	0.96[EUR][1000 genomes]
rs9971710	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9971811	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054573	chr12:85658602-86235433	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1035600	chr12:85661373-86235433	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1043253	chr12:85888151-86125364	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1054475	chr12:85985510-86175711	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv541561	chr12:85985510-86175711	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86096000-86105600	Weak transcription	Aorta	Aorta
2	chr12:86105200-86106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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