Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1746051	1.00[ASN][1000 genomes]
rs1746053	1.00[ASN][1000 genomes]
rs2146808	1.00[ASN][1000 genomes]
rs2760671	1.00[ASN][1000 genomes]
rs2760672	1.00[ASN][1000 genomes]
rs2802478	1.00[ASN][1000 genomes]
rs2802479	1.00[ASN][1000 genomes]
rs35155049	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35374150	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs549054	1.00[ASN][1000 genomes]
rs702363	1.00[ASN][1000 genomes]
rs71491034	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs768676	1.00[ASN][1000 genomes]
rs7918766	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs800309	1.00[ASN][1000 genomes]
rs800316	1.00[ASN][1000 genomes]
rs800318	1.00[ASN][1000 genomes]
rs800320	1.00[ASN][1000 genomes]
rs800324	1.00[ASN][1000 genomes]
rs800327	1.00[ASN][1000 genomes]
rs808972	1.00[ASN][1000 genomes]
rs809601	1.00[ASN][1000 genomes]
rs812331	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1043342	chr10:44650635-44682716	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr10:44650200-44659800	Weak transcription	Left Ventricle	heart

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