Variant report

Variant	rs7437622
Chromosome Location	chr4:166569327-166569328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10012405	0.84[ASN][1000 genomes]
rs10029541	0.80[ASN][1000 genomes]
rs11931542	0.92[ASN][1000 genomes]
rs11932029	0.84[ASN][1000 genomes]
rs11938725	0.94[ASN][1000 genomes]
rs1246904	0.86[ASN][1000 genomes]
rs1246905	0.94[ASN][1000 genomes]
rs1246906	0.86[ASN][1000 genomes]
rs1246908	0.93[ASN][1000 genomes]
rs1246910	0.94[ASN][1000 genomes]
rs1246918	0.93[ASN][1000 genomes]
rs1246920	0.94[ASN][1000 genomes]
rs12650088	0.82[ASN][1000 genomes]
rs1312880	0.94[ASN][1000 genomes]
rs17632084	0.88[ASN][1000 genomes]
rs17632233	0.84[ASN][1000 genomes]
rs1841210	0.86[ASN][1000 genomes]
rs1960435	0.94[ASN][1000 genomes]
rs2253129	0.86[ASN][1000 genomes]
rs2322266	0.86[ASN][1000 genomes]
rs2611205	0.82[ASN][1000 genomes]
rs2611209	0.84[ASN][1000 genomes]
rs2611211	0.85[ASN][1000 genomes]
rs2611212	1.00[ASN][1000 genomes]
rs2611214	1.00[ASN][1000 genomes]
rs2611215	0.92[ASN][1000 genomes]
rs2611216	0.92[ASN][1000 genomes]
rs2611218	1.00[ASN][1000 genomes]
rs2611219	0.89[ASN][1000 genomes]
rs2611220	1.00[ASN][1000 genomes]
rs2611221	0.92[ASN][1000 genomes]
rs2714828	0.92[ASN][1000 genomes]
rs2714829	0.92[ASN][1000 genomes]
rs2714831	1.00[ASN][1000 genomes]
rs2714833	0.92[ASN][1000 genomes]
rs2714834	0.92[ASN][1000 genomes]
rs2714835	1.00[ASN][1000 genomes]
rs2714836	1.00[ASN][1000 genomes]
rs2714837	0.92[ASN][1000 genomes]
rs2714839	0.90[ASN][1000 genomes]
rs28455937	0.84[ASN][1000 genomes]
rs28504666	0.84[ASN][1000 genomes]
rs28602943	0.84[ASN][1000 genomes]
rs4511957	0.86[ASN][1000 genomes]
rs4691212	0.90[CHD][hapmap];0.84[ASN][1000 genomes]
rs55989211	0.85[ASN][1000 genomes]
rs56396842	1.00[ASN][1000 genomes]
rs58230571	0.84[ASN][1000 genomes]
rs60551091	0.90[ASN][1000 genomes]
rs61702512	0.88[ASN][1000 genomes]
rs6536925	0.84[ASN][1000 genomes]
rs6536926	0.92[ASN][1000 genomes]
rs72631701	0.92[ASN][1000 genomes]
rs72631702	0.84[ASN][1000 genomes]
rs72635103	0.84[ASN][1000 genomes]
rs72635104	0.84[ASN][1000 genomes]
rs72635105	0.84[ASN][1000 genomes]
rs72635106	0.84[ASN][1000 genomes]
rs72635107	0.84[ASN][1000 genomes]
rs736675	0.94[ASN][1000 genomes]
rs73863250	0.84[ASN][1000 genomes]
rs73863253	0.84[ASN][1000 genomes]
rs73863254	0.84[ASN][1000 genomes]
rs764240	0.85[ASN][1000 genomes]
rs7675632	0.92[ASN][1000 genomes]
rs7696608	0.92[ASN][1000 genomes]
rs9308114	0.84[ASN][1000 genomes]
rs9992610	0.84[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
rs7437622	ANXA10	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166569200-166570000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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