Variant report

Variant	rs35220172
Chromosome Location	chr7:38965629-38965630
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1012976	1.00[ASN][1000 genomes]
rs10224856	1.00[ASN][1000 genomes]
rs10225415	1.00[ASN][1000 genomes]
rs10225550	0.81[EUR][1000 genomes]
rs10239904	0.90[EUR][1000 genomes]
rs10254354	1.00[ASN][1000 genomes]
rs10254873	0.81[EUR][1000 genomes]
rs10264217	0.90[EUR][1000 genomes]
rs10266279	0.80[EUR][1000 genomes]
rs10270427	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10270483	0.90[EUR][1000 genomes]
rs10951574	1.00[ASN][1000 genomes]
rs11983387	0.80[EUR][1000 genomes]
rs12701656	1.00[ASN][1000 genomes]
rs12701657	1.00[ASN][1000 genomes]
rs12701661	1.00[ASN][1000 genomes]
rs12701682	0.85[AFR][1000 genomes]
rs13224619	1.00[ASN][1000 genomes]
rs13224857	1.00[ASN][1000 genomes]
rs13229445	1.00[ASN][1000 genomes]
rs13235997	1.00[ASN][1000 genomes]
rs17240051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2040878	1.00[ASN][1000 genomes]
rs2079546	0.81[EUR][1000 genomes]
rs2189854	1.00[ASN][1000 genomes]
rs2190667	0.81[EUR][1000 genomes]
rs2214667	1.00[ASN][1000 genomes]
rs2214668	1.00[ASN][1000 genomes]
rs2215032	1.00[ASN][1000 genomes]
rs2245773	1.00[ASN][1000 genomes]
rs2286089	1.00[ASN][1000 genomes]
rs2286093	1.00[ASN][1000 genomes]
rs2286101	1.00[ASN][1000 genomes]
rs2392599	1.00[ASN][1000 genomes]
rs2392608	0.81[EUR][1000 genomes]
rs2392610	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34621392	1.00[ASN][1000 genomes]
rs34997080	1.00[ASN][1000 genomes]
rs35816439	1.00[ASN][1000 genomes]
rs35843038	1.00[ASN][1000 genomes]
rs4275134	0.88[EUR][1000 genomes]
rs4720300	1.00[ASN][1000 genomes]
rs4723780	1.00[ASN][1000 genomes]
rs4723781	1.00[ASN][1000 genomes]
rs4723784	1.00[ASN][1000 genomes]
rs4723787	1.00[ASN][1000 genomes]
rs4723802	0.83[EUR][1000 genomes]
rs4723804	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6462871	0.80[EUR][1000 genomes]
rs6462873	0.81[EUR][1000 genomes]
rs6462874	0.81[EUR][1000 genomes]
rs6947695	0.81[EUR][1000 genomes]
rs6949958	1.00[ASN][1000 genomes]
rs6951429	1.00[ASN][1000 genomes]
rs6960945	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6963090	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6964985	0.81[EUR][1000 genomes]
rs6967384	1.00[ASN][1000 genomes]
rs6971632	0.90[EUR][1000 genomes]
rs6974764	0.81[EUR][1000 genomes]
rs6975410	1.00[ASN][1000 genomes]
rs6976302	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6976579	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6978805	0.88[EUR][1000 genomes]
rs6979423	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73370730	1.00[ASN][1000 genomes]
rs757685	1.00[ASN][1000 genomes]
rs758088	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7782140	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7782277	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7783723	0.81[EUR][1000 genomes]
rs7784065	0.81[EUR][1000 genomes]
rs7784609	0.81[EUR][1000 genomes]
rs7787423	1.00[ASN][1000 genomes]
rs7789864	0.81[EUR][1000 genomes]
rs7793250	0.81[EUR][1000 genomes]
rs7799887	0.90[EUR][1000 genomes]
rs7802052	1.00[ASN][1000 genomes]
rs7803488	0.90[EUR][1000 genomes]
rs9638945	0.81[EUR][1000 genomes]
rs976352	1.00[ASN][1000 genomes]
rs9886108	0.81[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	nsv830967	chr7:38913837-39069253	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35220172	VPS41	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38965600-38968800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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