Variant report

Variant	rs10876941
Chromosome Location	chr12:57267216-57267217
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10735869	0.91[ASN][1000 genomes]
rs10783805	0.84[CHB][hapmap];0.82[JPT][hapmap]
rs10876943	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11172025	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11172033	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2888106	0.80[EUR][1000 genomes]
rs2888107	0.80[EUR][1000 genomes]
rs2888108	0.80[EUR][1000 genomes]
rs4254104	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4472974	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4477473	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4759036	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4759041	0.81[EUR][1000 genomes]
rs55812315	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61939604	0.81[EUR][1000 genomes]
rs7303219	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.88[MKK][hapmap];0.95[ASN][1000 genomes]
rs7305700	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7306442	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7314652	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7955918	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7956391	0.84[EUR][1000 genomes]
rs7959253	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7959654	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7959725	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7960137	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7960618	0.82[EUR][1000 genomes]
rs7961602	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7967940	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7972591	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7979655	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs840161	0.84[ASW][hapmap];0.85[CEU][hapmap]
rs9668259	0.83[AMR][1000 genomes];0.91[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	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs10876941	RDH16	cis	cerebellum	SCAN
rs10876941	ACVR1B	cis	parietal	SCAN
rs10876941	LRP1	cis	cerebellar cortex	BrainEAC
rs10876941	GALNT6	cis	parietal	SCAN
rs10876941	APOF	cis	parietal	SCAN
rs10876941	RAB5B	cis	parietal	SCAN
rs10876941	BIN2	cis	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57265400-57270000	Weak transcription	Liver	Liver
2	chr12:57265800-57267600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:57266800-57267400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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