Variant report

Variant	rs6471526
Chromosome Location	chr8:96328038-96328039
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11784608	1.00[CHD][hapmap]
rs13260234	1.00[ASN][1000 genomes]
rs13267037	1.00[ASN][1000 genomes]
rs13267333	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs13267612	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs13271205	1.00[ASN][1000 genomes]
rs13276926	1.00[ASN][1000 genomes]
rs1994794	0.87[ASW][hapmap];0.81[CEU][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34196697	1.00[ASN][1000 genomes]
rs34227899	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34289076	1.00[ASN][1000 genomes]
rs34389602	1.00[ASN][1000 genomes]
rs34463279	1.00[ASN][1000 genomes]
rs34861861	1.00[ASN][1000 genomes]
rs34962193	1.00[ASN][1000 genomes]
rs35141355	1.00[ASN][1000 genomes]
rs35175236	1.00[ASN][1000 genomes]
rs35195888	1.00[ASN][1000 genomes]
rs35273564	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35511040	1.00[ASN][1000 genomes]
rs35530445	1.00[ASN][1000 genomes]
rs35543354	1.00[ASN][1000 genomes]
rs35559164	1.00[ASN][1000 genomes]
rs35809593	1.00[ASN][1000 genomes]
rs36032317	1.00[ASN][1000 genomes]
rs36096184	1.00[ASN][1000 genomes]
rs55677759	1.00[ASN][1000 genomes]
rs56186143	1.00[ASN][1000 genomes]
rs56237137	1.00[ASN][1000 genomes]
rs57183551	1.00[ASN][1000 genomes]
rs58191899	1.00[ASN][1000 genomes]
rs58229316	1.00[ASN][1000 genomes]
rs58471124	1.00[ASN][1000 genomes]
rs58979833	1.00[ASN][1000 genomes]
rs59707579	1.00[ASN][1000 genomes]
rs60835162	1.00[ASN][1000 genomes]
rs61185934	1.00[ASN][1000 genomes]
rs61730929	1.00[ASN][1000 genomes]
rs61730932	1.00[ASN][1000 genomes]
rs61995709	1.00[ASN][1000 genomes]
rs61997199	1.00[ASN][1000 genomes]
rs7004873	1.00[ASN][1000 genomes]
rs71532351	1.00[ASN][1000 genomes]
rs71532352	1.00[ASN][1000 genomes]
rs71532353	1.00[ASN][1000 genomes]
rs73266490	1.00[ASN][1000 genomes]
rs73268303	1.00[ASN][1000 genomes]
rs73268328	1.00[ASN][1000 genomes]
rs73695429	1.00[ASN][1000 genomes]
rs73695431	1.00[ASN][1000 genomes]
rs73695432	1.00[ASN][1000 genomes]
rs73695433	1.00[ASN][1000 genomes]
rs73695435	1.00[ASN][1000 genomes]
rs73695436	1.00[ASN][1000 genomes]
rs73695437	1.00[ASN][1000 genomes]
rs73695438	1.00[ASN][1000 genomes]
rs73695439	1.00[ASN][1000 genomes]
rs7814173	1.00[ASN][1000 genomes]
rs7815085	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs7841828	1.00[ASN][1000 genomes]
rs894149	1.00[ASN][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	nsv429930	chr8:96317910-96454743	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6471526	RBM12B	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96326800-96328200	Enhancers	Brain Anterior Caudate	brain
2	chr8:96327000-96328200	Enhancers	Pancreas	Pancrea
3	chr8:96327000-96329800	Enhancers	Brain Substantia Nigra	brain
4	chr8:96327200-96330200	Enhancers	Brain Hippocampus Middle	brain
5	chr8:96327400-96330200	Enhancers	Brain Cingulate Gyrus	brain
6	chr8:96327600-96328200	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr8:96327600-96329000	Enhancers	Brain Germinal Matrix	brain
8	chr8:96328000-96328800	Weak transcription	Brain Angular Gyrus	brain

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