Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10497908	0.81[ASN][1000 genomes]
rs12996332	0.81[ASN][1000 genomes]
rs13005342	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13009129	0.81[ASN][1000 genomes]
rs13024405	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13032937	1.00[ASN][1000 genomes]
rs13420017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13421435	1.00[ASN][1000 genomes]
rs13426261	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16824865	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16841488	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16841490	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16841492	1.00[ASN][1000 genomes]
rs16841494	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16841506	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34303255	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34546401	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35962803	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60116276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61183844	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6435467	1.00[ASN][1000 genomes]
rs6749585	1.00[ASN][1000 genomes]
rs7561893	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7587825	1.00[AMR][1000 genomes];1.00[ASN][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	nsv1005292	chr2:209470753-209631662	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv2756959	chr2:209472551-209551952	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2759112	chr2:209472551-209551952	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv875753	chr2:209474223-209517915	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209482400-209485400	Enhancers	Fetal Heart	heart
2	chr2:209482400-209485600	Enhancers	K562	blood
3	chr2:209484200-209485000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr2:209484400-209485000	Enhancers	Pancreas	Pancrea

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