Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10838445	0.86[EUR][1000 genomes]
rs10838451	0.87[EUR][1000 genomes]
rs10838456	1.00[ASN][1000 genomes]
rs11038408	1.00[ASN][1000 genomes]
rs11038412	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11607009	1.00[ASN][1000 genomes]
rs4755319	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4755320	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755321	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755977	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4755978	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61882561	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61882562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61882563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61882566	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61882568	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7484258	0.83[EUR][1000 genomes]
rs7943277	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7943376	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7952613	0.85[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	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr11:45377600-45380200	Weak transcription	Aorta	Aorta
2	chr11:45377800-45378800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr11:45378000-45387800	Weak transcription	Lung	lung
4	chr11:45378200-45378800	Enhancers	Brain Germinal Matrix	brain
5	chr11:45378200-45387200	Weak transcription	Brain Anterior Caudate	brain
6	chr11:45378200-45387800	Weak transcription	Fetal Brain Male	brain

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