Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10157869	1.00[EUR][1000 genomes]
rs10159030	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1114004	1.00[EUR][1000 genomes]
rs13373836	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13374961	1.00[ASN][1000 genomes]
rs13374962	1.00[ASN][1000 genomes]
rs17131669	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131670	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131671	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131672	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131673	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131674	1.00[ASN][1000 genomes]
rs17131676	1.00[EUR][1000 genomes]
rs17131677	1.00[EUR][1000 genomes]
rs4394666	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59078677	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60684469	1.00[ASN][1000 genomes]
rs61318253	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6673190	1.00[EUR][1000 genomes]
rs7515224	1.00[ASN][1000 genomes]
rs7519363	1.00[ASN][1000 genomes]
rs7539571	1.00[ASN][1000 genomes]
rs7552766	1.00[ASN][1000 genomes]
rs9324344	1.00[EUR][1000 genomes]
rs9324345	1.00[EUR][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	nsv1008602	chr1:93176811-93640808	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93350000-93366400	Weak transcription	Thymus	Thymus
2	chr1:93361800-93366800	Weak transcription	Aorta	Aorta
3	chr1:93363200-93364400	Enhancers	Primary B cells from peripheral blood	blood

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