Variant report

Variant	rs4402886
Chromosome Location	chr3:60664177-60664178
allele	C/T
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:83)

rs_ID	r²[population]
rs11921025	0.88[EUR][1000 genomes]
rs11922545	0.85[YRI][hapmap]
rs11923145	0.82[EUR][1000 genomes]
rs11923899	0.90[YRI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11926456	0.88[EUR][1000 genomes]
rs11928674	0.88[EUR][1000 genomes]
rs13314853	0.94[ASN][1000 genomes]
rs13321532	0.88[EUR][1000 genomes]
rs17063317	1.00[CHB][hapmap]
rs17063781	0.94[YRI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4393862	0.82[EUR][1000 genomes]
rs57004000	0.88[EUR][1000 genomes]
rs58195903	0.82[EUR][1000 genomes]
rs58745931	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62249155	0.88[ASN][1000 genomes]
rs62249304	0.82[EUR][1000 genomes]
rs62251489	0.94[ASN][1000 genomes]
rs62251492	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs62251493	0.97[ASN][1000 genomes]
rs62251494	0.97[ASN][1000 genomes]
rs62251500	0.83[AFR][1000 genomes]
rs62251502	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62251532	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62251534	0.88[EUR][1000 genomes]
rs62251535	0.88[EUR][1000 genomes]
rs62251537	0.88[EUR][1000 genomes]
rs62251538	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62251539	0.88[EUR][1000 genomes]
rs62251540	0.88[EUR][1000 genomes]
rs62251541	0.88[EUR][1000 genomes]
rs6446150	0.88[EUR][1000 genomes]
rs6772346	0.88[EUR][1000 genomes]
rs6784732	1.00[CHB][hapmap];0.85[YRI][hapmap];0.91[ASN][1000 genomes]
rs6789900	0.88[EUR][1000 genomes]
rs6793104	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6797892	0.82[EUR][1000 genomes]
rs72872798	0.94[ASN][1000 genomes]
rs72875002	0.88[EUR][1000 genomes]
rs7618351	0.88[EUR][1000 genomes]
rs7636178	0.88[EUR][1000 genomes]
rs7638652	0.88[EUR][1000 genomes]
rs7638754	0.88[EUR][1000 genomes]
rs7641604	0.88[EUR][1000 genomes]
rs7642546	0.94[EUR][1000 genomes]
rs9311772	0.88[EUR][1000 genomes]
rs9311773	0.88[EUR][1000 genomes]
rs9810266	0.94[EUR][1000 genomes]
rs9811304	0.88[EUR][1000 genomes]
rs9814237	0.88[EUR][1000 genomes]
rs9816751	0.88[EUR][1000 genomes]
rs9816956	0.88[EUR][1000 genomes]
rs9818734	0.88[EUR][1000 genomes]
rs9824756	0.88[EUR][1000 genomes]
rs9826128	0.82[EUR][1000 genomes]
rs9826570	0.82[EUR][1000 genomes]
rs9827312	0.82[EUR][1000 genomes]
rs9827340	0.82[EUR][1000 genomes]
rs9827546	0.94[ASN][1000 genomes]
rs9828898	0.88[EUR][1000 genomes]
rs9830759	0.94[EUR][1000 genomes]
rs9832938	0.88[EUR][1000 genomes]
rs9834653	0.88[EUR][1000 genomes]
rs9838172	0.88[EUR][1000 genomes]
rs9838335	0.88[EUR][1000 genomes]
rs9838669	0.88[EUR][1000 genomes]
rs9839019	0.82[EUR][1000 genomes]
rs9839778	0.88[EUR][1000 genomes]
rs9840107	0.88[EUR][1000 genomes]
rs9840473	0.88[EUR][1000 genomes]
rs9844497	0.82[EUR][1000 genomes]
rs9845813	0.88[EUR][1000 genomes]
rs9861551	0.88[EUR][1000 genomes]
rs9861707	0.88[EUR][1000 genomes]
rs9866844	0.88[EUR][1000 genomes]
rs9868891	0.94[EUR][1000 genomes]
rs9872622	0.88[EUR][1000 genomes]
rs9874852	0.88[EUR][1000 genomes]
rs9875027	0.88[EUR][1000 genomes]
rs9876876	0.82[EUR][1000 genomes]
rs9878248	0.88[EUR][1000 genomes]
rs9878383	0.88[EUR][1000 genomes]
rs9881065	0.88[EUR][1000 genomes]
rs9882477	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60658600-60664400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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