Variant report

Variant	rs9662174
Chromosome Location	chr1:171652144-171652145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1001373	0.81[EUR][1000 genomes]
rs1052676	0.83[EUR][1000 genomes]
rs10903	0.83[EUR][1000 genomes]
rs10913475	0.87[ASN][1000 genomes]
rs10913489	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913490	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913492	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913511	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10913514	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10913529	0.81[EUR][1000 genomes]
rs11576221	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11578179	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11579698	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11580415	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11583920	0.81[EUR][1000 genomes]
rs11799420	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11801846	0.82[EUR][1000 genomes]
rs11802265	0.81[ASN][1000 genomes]
rs11803174	0.82[EUR][1000 genomes]
rs11808099	0.81[EUR][1000 genomes]
rs11811780	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12118409	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12119553	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12123727	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12125429	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12127026	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12128536	0.82[EUR][1000 genomes]
rs12132221	0.81[EUR][1000 genomes]
rs15655	0.83[EUR][1000 genomes]
rs3766653	0.80[EUR][1000 genomes]
rs55670848	0.81[EUR][1000 genomes]
rs56091821	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56220250	0.82[AMR][1000 genomes]
rs56345529	0.90[ASN][1000 genomes]
rs58455759	0.82[EUR][1000 genomes]
rs6656003	0.81[EUR][1000 genomes]
rs6659874	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6667559	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669263	0.81[EUR][1000 genomes]
rs6678890	0.81[EUR][1000 genomes]
rs6679354	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6687922	0.87[ASN][1000 genomes]
rs6688018	0.89[ASN][1000 genomes]
rs7528057	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7536436	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7536543	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9661596	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9662853	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv12447	chr1:171556291-171726822	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv872544	chr1:171616822-171654968	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9662174	VAMP4	Cis_1M	lymphoblastoid	RTeQTL
rs9662174	VAMP4	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171647800-171652800	Weak transcription	K562	blood

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