Variant report

Variant	rs11756183
Chromosome Location	chr6:79080437-79080438
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11751193	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11753607	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11754432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11755278	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11758756	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425493	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425494	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425498	0.80[EUR][1000 genomes]
rs62425539	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425540	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425541	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425542	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425543	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425544	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425545	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425546	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62425547	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62426477	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758064	chr6:78795880-79193468	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2759447	chr6:78795880-79193468	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv428149	chr6:78890476-79099763	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2757181	chr6:78944539-79094007	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv821650	chr6:79002204-79095287	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1018006	chr6:79003806-79228498	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv7931	chr6:79078579-79080460	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	chr6:79080200-79080800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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