Variant report

Variant	rs764240
Chromosome Location	chr4:166575899-166575900
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10012405	0.81[CHB][hapmap];0.83[ASN][1000 genomes]
rs10029541	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11931542	0.90[ASN][1000 genomes]
rs11932029	0.83[ASN][1000 genomes]
rs11938725	0.81[ASN][1000 genomes]
rs1246904	0.88[ASN][1000 genomes]
rs1246905	0.81[ASN][1000 genomes]
rs1246906	0.88[ASN][1000 genomes]
rs1246908	0.80[ASN][1000 genomes]
rs1246910	0.81[ASN][1000 genomes]
rs1246918	0.80[ASN][1000 genomes]
rs1246920	0.81[ASN][1000 genomes]
rs12650088	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1312880	0.81[ASN][1000 genomes]
rs1459507	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17632233	0.83[ASN][1000 genomes]
rs1841210	0.88[ASN][1000 genomes]
rs1960435	0.81[ASN][1000 genomes]
rs2253129	0.88[ASN][1000 genomes]
rs2322266	0.88[ASN][1000 genomes]
rs2611205	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2611209	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2611211	0.98[ASN][1000 genomes]
rs2611212	0.85[ASN][1000 genomes]
rs2611214	0.85[ASN][1000 genomes]
rs2611215	0.93[ASN][1000 genomes]
rs2611216	0.93[ASN][1000 genomes]
rs2611218	0.85[ASN][1000 genomes]
rs2611219	0.90[ASN][1000 genomes]
rs2611220	0.85[ASN][1000 genomes]
rs2611221	0.93[ASN][1000 genomes]
rs2714828	0.93[ASN][1000 genomes]
rs2714829	0.93[ASN][1000 genomes]
rs2714831	0.85[ASN][1000 genomes]
rs2714833	0.93[ASN][1000 genomes]
rs2714834	0.93[ASN][1000 genomes]
rs2714835	0.85[ASN][1000 genomes]
rs2714836	0.85[ASN][1000 genomes]
rs2714837	0.93[ASN][1000 genomes]
rs2714839	0.91[ASN][1000 genomes]
rs28455937	0.82[ASN][1000 genomes]
rs28504666	0.83[ASN][1000 genomes]
rs28602943	0.83[ASN][1000 genomes]
rs4511957	0.89[ASN][1000 genomes]
rs4691212	0.81[CHB][hapmap];0.97[CHD][hapmap];0.83[ASN][1000 genomes]
rs56396842	0.85[ASN][1000 genomes]
rs58230571	0.83[ASN][1000 genomes]
rs60551091	0.88[ASN][1000 genomes]
rs61702512	0.86[ASN][1000 genomes]
rs6536925	0.86[ASN][1000 genomes]
rs6536926	0.93[ASN][1000 genomes]
rs72631701	0.90[ASN][1000 genomes]
rs72631702	0.83[ASN][1000 genomes]
rs72635103	0.83[ASN][1000 genomes]
rs72635104	0.83[ASN][1000 genomes]
rs72635105	0.83[ASN][1000 genomes]
rs72635106	0.83[ASN][1000 genomes]
rs72635107	0.83[ASN][1000 genomes]
rs736675	0.81[ASN][1000 genomes]
rs73863250	0.83[ASN][1000 genomes]
rs73863253	0.83[ASN][1000 genomes]
rs73863254	0.83[ASN][1000 genomes]
rs7437622	0.85[ASN][1000 genomes]
rs7675632	0.93[ASN][1000 genomes]
rs7696608	0.93[ASN][1000 genomes]
rs9308114	0.83[ASN][1000 genomes]
rs9992610	0.82[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	nsv830141	chr4:166502908-166689626	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1028337	chr4:166544699-166659468	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv537338	chr4:166544699-166659468	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3486584	chr4:166565013-166680227	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv3486585	chr4:166565013-166680227	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs764240	NPY1R	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166570000-166584200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:166574200-166578600	Enhancers	HepG2	liver
3	chr4:166575400-166576400	Enhancers	Liver	Liver
4	chr4:166575800-166576000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:166575800-166579000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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