Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11930355	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17026072	1.00[ASN][1000 genomes]
rs17026111	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2164997	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4301085	1.00[AMR][1000 genomes]
rs4510455	1.00[AMR][1000 genomes]
rs56208724	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58022888	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59242740	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59690219	1.00[AMR][1000 genomes]
rs61133328	1.00[AMR][1000 genomes]
rs72951795	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72951797	1.00[AMR][1000 genomes]
rs72951801	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72953611	1.00[AMR][1000 genomes]
rs72953613	1.00[AMR][1000 genomes]
rs72953615	1.00[AMR][1000 genomes]
rs72953627	1.00[AMR][1000 genomes]
rs72953659	1.00[AMR][1000 genomes]
rs72953662	1.00[AMR][1000 genomes]
rs72953666	1.00[AMR][1000 genomes]
rs72953668	1.00[AMR][1000 genomes]
rs72953669	1.00[AMR][1000 genomes]
rs72966027	1.00[AMR][1000 genomes]
rs72966028	1.00[AMR][1000 genomes]
rs72966031	1.00[AMR][1000 genomes]
rs72966091	1.00[AMR][1000 genomes]
rs72966101	1.00[AMR][1000 genomes]
rs72967931	1.00[AMR][1000 genomes]
rs73859724	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7678170	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022438	chr4:150066349-150196711	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880248	chr4:150092178-150200706	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv880249	chr4:150156579-150280221	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1016977	chr4:150173255-150605595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv537298	chr4:150173255-150605595	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr4:150186800-150187400	Enhancers	Fetal Lung	lung

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