Variant report

Variant	rs73146008
Chromosome Location	chr3:82342596-82342597
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12632087	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6763406	0.91[ASN][1000 genomes]
rs6781784	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73135762	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73136194	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73136200	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73138120	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138123	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138125	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138134	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138138	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138148	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73140170	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73140171	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73142107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73142109	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73142114	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73142115	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73142118	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144102	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73146013	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73148052	0.91[ASN][1000 genomes]
rs73148056	0.91[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	nsv877041	chr3:82074024-82363196	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1008429	chr3:82089650-82510536	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv432460	chr3:82107110-82508010	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1013820	chr3:82175705-82968181	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr3:82342000-82343400	Enhancers	GM12878-XiMat	blood

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