Variant report

Variant	rs34320519
Chromosome Location	chr1:171263558-171263559
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:171258018..171259639-chr1:171260854..171263633,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10399602	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10399952	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10798297	0.94[ASN][1000 genomes]
rs10912672	0.85[ASN][1000 genomes]
rs10912673	0.85[ASN][1000 genomes]
rs10912713	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10912714	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10912723	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10912736	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1126692	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11484641	0.85[ASN][1000 genomes]
rs11484642	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11487396	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12057955	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12058402	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12059179	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12062692	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12068552	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12070766	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12072043	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12077231	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12077755	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12079141	1.00[ASN][1000 genomes]
rs12080449	1.00[ASN][1000 genomes]
rs12081291	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12091482	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12092985	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12094878	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12141555	0.94[ASN][1000 genomes]
rs12354390	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12726624	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12729885	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12730181	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12742008	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12745080	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12747080	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12757839	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13376631	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16864302	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16864387	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17581251	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2006986	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2076322	1.00[ASN][1000 genomes]
rs2092311	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2284131	0.80[ASN][1000 genomes]
rs28741369	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34118031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4607925	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55949630	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6670639	0.85[ASN][1000 genomes]
rs6674596	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs742350	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs742351	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7512853	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7519999	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7539057	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7541377	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	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
3	esv10193	chr1:171128845-171414611	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv831882	chr1:171166224-171326083	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs34320519	FMO4	cis	Heart Left Ventricle	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171261600-171266400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:171261800-171266200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:171262600-171264000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:171263000-171264400	Enhancers	Fetal Intestine Small	intestine
5	chr1:171263200-171263600	Weak transcription	NHDF-Ad	bronchial
6	chr1:171263400-171264000	Weak transcription	Fetal Intestine Large	intestine
7	chr1:171263400-171264400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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