Variant report

Variant	rs10111851
Chromosome Location	chr8:36049185-36049186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10103388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10503987	1.00[EUR][1000 genomes]
rs1108072	0.96[ASN][1000 genomes]
rs12674672	0.92[ASN][1000 genomes]
rs16884907	1.00[EUR][1000 genomes]
rs16884936	1.00[EUR][1000 genomes]
rs16884940	1.00[EUR][1000 genomes]
rs16884942	1.00[EUR][1000 genomes]
rs16884948	1.00[EUR][1000 genomes]
rs16884954	1.00[EUR][1000 genomes]
rs16884958	1.00[EUR][1000 genomes]
rs16884962	1.00[EUR][1000 genomes]
rs16884965	1.00[EUR][1000 genomes]
rs16884968	1.00[EUR][1000 genomes]
rs16884969	1.00[EUR][1000 genomes]
rs2017573	0.84[AFR][1000 genomes]
rs2702470	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2702491	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2702496	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843885	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2843886	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843887	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28576407	0.80[AFR][1000 genomes]
rs57959662	1.00[EUR][1000 genomes]
rs58562297	1.00[EUR][1000 genomes]
rs589543	0.86[ASN][1000 genomes]
rs59452926	1.00[EUR][1000 genomes]
rs60158913	1.00[EUR][1000 genomes]
rs60587267	1.00[EUR][1000 genomes]
rs6985277	0.85[AFR][1000 genomes]
rs6991021	1.00[EUR][1000 genomes]
rs6991760	0.89[ASN][1000 genomes]
rs7006112	1.00[EUR][1000 genomes]
rs73578590	1.00[EUR][1000 genomes]
rs73580494	0.80[AFR][1000 genomes]
rs73580606	1.00[EUR][1000 genomes]
rs73580614	1.00[EUR][1000 genomes]
rs73580674	1.00[EUR][1000 genomes]
rs73582414	1.00[EUR][1000 genomes]
rs73582415	1.00[EUR][1000 genomes]
rs73582417	1.00[EUR][1000 genomes]
rs73582420	1.00[EUR][1000 genomes]
rs73582422	1.00[EUR][1000 genomes]
rs73582427	1.00[EUR][1000 genomes]
rs73582428	1.00[EUR][1000 genomes]
rs73582429	1.00[EUR][1000 genomes]
rs73582431	1.00[EUR][1000 genomes]
rs73582493	1.00[EUR][1000 genomes]
rs73582495	1.00[EUR][1000 genomes]
rs73582496	1.00[EUR][1000 genomes]
rs73582502	1.00[EUR][1000 genomes]
rs73584406	1.00[EUR][1000 genomes]
rs7822201	0.83[ASN][1000 genomes]
rs7827472	0.89[AFR][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	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1024552	chr8:35655964-36210907	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539548	chr8:35655964-36210907	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv890718	chr8:35948467-36224134	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr8:36046400-36049600	Weak transcription	Adipose Nuclei	Adipose

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