Variant report

Variant	rs13151714
Chromosome Location	chr4:143972993-143972994
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10015475	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1104696	0.90[ASN][1000 genomes]
rs1104697	0.90[ASN][1000 genomes]
rs1105832	0.90[ASN][1000 genomes]
rs11721635	0.90[ASN][1000 genomes]
rs11728404	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11731763	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11736977	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11933570	0.90[ASN][1000 genomes]
rs12505602	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12507913	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12640644	0.90[ASN][1000 genomes]
rs12644403	0.90[ASN][1000 genomes]
rs13115992	0.89[ASN][1000 genomes]
rs13126432	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13134924	0.90[ASN][1000 genomes]
rs13139088	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1355259	1.00[JPT][hapmap]
rs1510141	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1510142	0.90[ASN][1000 genomes]
rs1588410	0.90[ASN][1000 genomes]
rs1588411	0.90[ASN][1000 genomes]
rs17017174	0.90[ASN][1000 genomes]
rs17017180	0.90[ASN][1000 genomes]
rs17017183	0.90[ASN][1000 genomes]
rs17017184	0.90[ASN][1000 genomes]
rs1949068	0.90[ASN][1000 genomes]
rs1949069	0.90[ASN][1000 genomes]
rs28431796	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28496540	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28623359	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28644452	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28660021	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28660573	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2874933	0.90[ASN][1000 genomes]
rs28817081	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35342016	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3967114	0.90[ASN][1000 genomes]
rs4054820	0.90[ASN][1000 genomes]
rs4074924	0.90[ASN][1000 genomes]
rs4074925	0.90[ASN][1000 genomes]
rs4074926	0.90[ASN][1000 genomes]
rs4076451	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4077294	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4234880	0.90[ASN][1000 genomes]
rs4234884	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4323053	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4327439	0.90[ASN][1000 genomes]
rs4367125	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4407448	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4473614	0.90[ASN][1000 genomes]
rs4485768	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4524335	0.94[ASN][1000 genomes]
rs4619836	1.00[JPT][hapmap]
rs4690713	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4690714	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4690749	0.90[ASN][1000 genomes]
rs4690752	0.90[ASN][1000 genomes]
rs4690755	1.00[JPT][hapmap]
rs4690757	0.94[ASN][1000 genomes]
rs4690758	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690759	0.84[ASN][1000 genomes]
rs4690760	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690765	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57921755	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58401084	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59799467	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs66633688	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66750280	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6821582	0.90[ASN][1000 genomes]
rs6821603	0.90[ASN][1000 genomes]
rs6821648	0.90[ASN][1000 genomes]
rs72615966	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7657896	0.88[ASN][1000 genomes]
rs7676293	0.90[ASN][1000 genomes]
rs7681219	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7685713	0.90[ASN][1000 genomes]
rs7685774	0.90[ASN][1000 genomes]
rs7686660	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs955722	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9985884	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9991766	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1033285	chr4:143884298-144010784	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
2	nsv537288	chr4:143884298-144010784	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
3	nsv880176	chr4:143929235-144027729	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1034895	chr4:143945139-144079655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143972400-143973400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:143972600-143973000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:143972600-143973000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr4:143972600-143973400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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