Variant report

Variant	rs724929
Chromosome Location	chr3:56217454-56217455
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10433621	0.87[ASN][1000 genomes]
rs1078309	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs1078310	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap];0.89[ASN][1000 genomes]
rs12486927	0.82[ASN][1000 genomes]
rs12492055	0.86[ASN][1000 genomes]
rs1376984	0.86[ASW][hapmap];0.86[CEU][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs1452217	0.89[ASN][1000 genomes]
rs17056646	0.86[ASN][1000 genomes]
rs17732598	0.89[ASN][1000 genomes]
rs4974120	0.89[ASN][1000 genomes]
rs4974121	0.87[ASN][1000 genomes]
rs4974123	0.84[ASN][1000 genomes]
rs4974173	0.90[JPT][hapmap]
rs4974175	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4974176	0.89[ASN][1000 genomes]
rs4974179	0.86[ASN][1000 genomes]
rs4974180	0.89[ASN][1000 genomes]
rs55849756	0.86[ASN][1000 genomes]
rs60383545	0.87[ASN][1000 genomes]
rs6445770	0.90[JPT][hapmap]
rs6764295	0.82[CHD][hapmap];0.90[JPT][hapmap];0.82[MEX][hapmap];0.82[ASN][1000 genomes]
rs6779122	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6782034	0.89[ASN][1000 genomes]
rs6783356	0.86[ASN][1000 genomes]
rs6786058	0.86[ASN][1000 genomes]
rs6787104	0.83[CEU][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs6801342	0.86[ASN][1000 genomes]
rs6803165	0.87[ASN][1000 genomes]
rs72870171	0.82[ASN][1000 genomes]
rs755321	1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[ASN][1000 genomes]
rs7613726	0.86[ASN][1000 genomes]
rs7628255	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7644153	0.81[ASN][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	nsv1009709	chr3:56000827-56294945	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs724929	ARF4	cis	parietal	SCAN
rs724929	FLNB	cis	cerebellum	SCAN
rs724929	ERC2	cis	cerebellum	SCAN
rs724929	MUSTN1	cis	cerebellum	SCAN
rs724929	C3orf63	cis	cerebellum	SCAN
rs724929	C3orf51	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56211800-56222400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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