Variant report

Variant	rs6492232
Chromosome Location	chr13:110585170-110585171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1556574	0.82[ASN][1000 genomes]
rs1760599	0.82[ASN][1000 genomes]
rs1763034	0.82[ASN][1000 genomes]
rs1763035	0.82[ASN][1000 genomes]
rs1763036	0.82[ASN][1000 genomes]
rs1763037	0.82[ASN][1000 genomes]
rs1763038	0.82[ASN][1000 genomes]
rs1855440	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1932416	0.82[ASN][1000 genomes]
rs1953173	0.81[ASN][1000 genomes]
rs336205	0.82[ASN][1000 genomes]
rs336206	0.82[ASN][1000 genomes]
rs336207	0.82[ASN][1000 genomes]
rs336208	0.82[ASN][1000 genomes]
rs367400	0.82[ASN][1000 genomes]
rs371316	0.81[ASN][1000 genomes]
rs373872	0.82[ASN][1000 genomes]
rs378035	0.81[ASN][1000 genomes]
rs379193	0.82[ASN][1000 genomes]
rs384608	0.82[ASN][1000 genomes]
rs387811	0.81[ASN][1000 genomes]
rs392244	0.82[ASN][1000 genomes]
rs412905	0.81[ASN][1000 genomes]
rs416090	0.82[ASN][1000 genomes]
rs424480	0.82[ASN][1000 genomes]
rs426171	0.81[ASN][1000 genomes]
rs426839	0.82[ASN][1000 genomes]
rs431199	0.81[ASN][1000 genomes]
rs434999	0.82[ASN][1000 genomes]
rs444409	0.82[ASN][1000 genomes]
rs56183751	0.82[ASN][1000 genomes]
rs66895129	0.81[ASN][1000 genomes]
rs693404	0.82[ASN][1000 genomes]
rs7321836	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7491948	0.82[ASN][1000 genomes]
rs7491951	0.81[ASN][1000 genomes]
rs7982038	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7982666	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7991082	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7991265	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7994830	0.82[ASN][1000 genomes]
rs7995631	0.82[ASN][1000 genomes]
rs8000780	0.82[ASN][1000 genomes]
rs8001698	0.82[ASN][1000 genomes]
rs9555645	0.82[ASN][1000 genomes]
rs9555646	0.82[ASN][1000 genomes]
rs9555647	0.82[ASN][1000 genomes]
rs9559671	0.82[ASN][1000 genomes]
rs9559675	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9588050	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9634471	0.82[ASN][1000 genomes]
rs9634472	0.82[ASN][1000 genomes]
rs9634473	0.82[ASN][1000 genomes]
rs9634474	0.82[ASN][1000 genomes]
rs9634584	0.82[ASN][1000 genomes]
rs9634585	0.82[ASN][1000 genomes]
rs9634586	0.82[ASN][1000 genomes]
rs969718	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][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	nsv832719	chr13:110512259-110655883	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110566800-110590400	Weak transcription	Aorta	Aorta
2	chr13:110571000-110586000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:110584400-110586200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:110585000-110586200	Enhancers	Brain Germinal Matrix	brain

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