Variant report

Variant	rs73087684
Chromosome Location	chr12:44416728-44416729
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10736018	0.81[EUR][1000 genomes]
rs10785492	0.81[EUR][1000 genomes]
rs10880616	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10880617	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11182375	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182384	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182385	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182396	0.86[EUR][1000 genomes]
rs11182402	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11182404	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182405	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12099769	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12230287	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12296857	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12301507	0.83[AMR][1000 genomes]
rs12313365	0.86[EUR][1000 genomes]
rs1532218	0.83[AMR][1000 genomes]
rs1565620	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17093993	0.83[AMR][1000 genomes]
rs17094013	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1976211	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2407788	0.81[EUR][1000 genomes]
rs2407791	0.83[AMR][1000 genomes]
rs3929354	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55641600	0.83[AMR][1000 genomes]
rs55756710	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55773976	0.83[AMR][1000 genomes]
rs55834309	0.83[AMR][1000 genomes]
rs55917469	0.83[AMR][1000 genomes]
rs56011342	0.83[AMR][1000 genomes]
rs56081380	0.83[AMR][1000 genomes]
rs56114967	0.83[AMR][1000 genomes]
rs56198335	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56227915	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56337317	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56355753	0.83[AMR][1000 genomes]
rs6582494	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6582495	1.00[ASN][1000 genomes]
rs7132451	0.83[AMR][1000 genomes]
rs73085788	0.83[AMR][1000 genomes]
rs73087603	0.83[AMR][1000 genomes]
rs73087605	0.83[AMR][1000 genomes]
rs73087610	0.83[AMR][1000 genomes]
rs73087626	0.83[AMR][1000 genomes]
rs73087687	0.83[AMR][1000 genomes]
rs73087696	0.83[AMR][1000 genomes]
rs73087700	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73089723	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73089727	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73089730	0.83[AMR][1000 genomes]
rs73089748	0.83[AMR][1000 genomes]
rs73089752	0.83[AMR][1000 genomes]
rs73089753	0.83[AMR][1000 genomes]
rs73091736	0.83[AMR][1000 genomes]
rs73091745	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7311778	0.83[AMR][1000 genomes]
rs7312422	0.81[EUR][1000 genomes]
rs7959226	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7960478	0.83[AMR][1000 genomes]
rs7980005	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9783507	0.83[AMR][1000 genomes]
rs9919676	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9919711	0.83[AMR][1000 genomes]
rs9919742	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832390	chr12:44318071-44512114	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1041188	chr12:44331098-44528712	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832391	chr12:44394137-44552555	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44390800-44439200	Weak transcription	Esophagus	oesophagus
2	chr12:44402000-44432200	Weak transcription	Aorta	Aorta
3	chr12:44404000-44422600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:44404200-44422800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:44415800-44418200	Weak transcription	Fetal Brain Male	brain
6	chr12:44416400-44417000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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