Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10154838	1.00[EUR][1000 genomes]
rs17009055	0.88[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17009064	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17009069	1.00[AMR][1000 genomes]
rs28822992	1.00[EUR][1000 genomes]
rs3911497	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56165442	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56330701	1.00[AMR][1000 genomes]
rs56413975	1.00[AMR][1000 genomes]
rs57852338	1.00[EUR][1000 genomes]
rs58049694	1.00[AMR][1000 genomes]
rs58497066	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58525325	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60086939	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60352620	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60359281	1.00[EUR][1000 genomes]
rs61350442	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73819308	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73819309	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73819310	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73819522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73819961	1.00[AMR][1000 genomes]
rs7619515	1.00[EUR][1000 genomes]
rs9811766	1.00[EUR][1000 genomes]
rs9826648	1.00[EUR][1000 genomes]
rs9831866	1.00[ASW][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9852842	1.00[EUR][1000 genomes]
rs9874764	1.00[EUR][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	nsv1006471	chr3:21385627-21596955	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1010460	chr3:21516810-21839871	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3426590	chr3:21593997-21613071	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21574000-21602000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:21585000-21601600	Weak transcription	Fetal Stomach	stomach
3	chr3:21585800-21602000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:21588600-21603200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:21588600-21604600	Weak transcription	Aorta	Aorta
6	chr3:21593000-21606800	Weak transcription	K562	blood
7	chr3:21596400-21606800	Weak transcription	Psoas Muscle	Psoas

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