Variant report

Variant	rs2666117
Chromosome Location	chr4:28476701-28476702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10021733	0.82[ASN][1000 genomes]
rs12501893	0.90[ASN][1000 genomes]
rs12505899	0.90[ASN][1000 genomes]
rs12641531	0.82[ASN][1000 genomes]
rs12648642	0.82[ASN][1000 genomes]
rs1303816	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1303817	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1303818	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1303819	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13123915	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13125329	1.00[ASN][1000 genomes]
rs13132764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13147296	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1514126	0.90[ASN][1000 genomes]
rs1514128	0.90[ASN][1000 genomes]
rs1514129	0.82[ASN][1000 genomes]
rs167104	0.90[ASN][1000 genomes]
rs1708967	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs182378	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2221775	1.00[ASN][1000 genomes]
rs2248575	0.82[ASN][1000 genomes]
rs2250259	0.80[CEU][hapmap]
rs2458606	0.90[ASN][1000 genomes]
rs2458607	0.90[ASN][1000 genomes]
rs2458608	0.90[ASN][1000 genomes]
rs2458613	0.90[ASN][1000 genomes]
rs2458614	0.90[ASN][1000 genomes]
rs2458616	0.90[ASN][1000 genomes]
rs2458617	0.90[ASN][1000 genomes]
rs2458618	0.90[ASN][1000 genomes]
rs2458619	0.82[ASN][1000 genomes]
rs2458624	0.90[ASN][1000 genomes]
rs2458626	0.82[ASN][1000 genomes]
rs2458627	0.82[ASN][1000 genomes]
rs2458628	0.82[ASN][1000 genomes]
rs2458630	0.82[ASN][1000 genomes]
rs2471685	0.82[ASN][1000 genomes]
rs2471687	0.82[ASN][1000 genomes]
rs2471689	0.82[ASN][1000 genomes]
rs2471690	0.82[ASN][1000 genomes]
rs2471691	0.82[ASN][1000 genomes]
rs2471692	0.82[ASN][1000 genomes]
rs2471703	0.82[ASN][1000 genomes]
rs2471705	0.82[ASN][1000 genomes]
rs2471707	0.82[ASN][1000 genomes]
rs2471709	0.82[ASN][1000 genomes]
rs2471710	0.82[ASN][1000 genomes]
rs2471711	0.82[ASN][1000 genomes]
rs2471715	0.90[ASN][1000 genomes]
rs2471717	0.90[ASN][1000 genomes]
rs2471718	0.90[ASN][1000 genomes]
rs2471719	0.90[ASN][1000 genomes]
rs2471720	0.90[ASN][1000 genomes]
rs2471721	0.90[ASN][1000 genomes]
rs28406281	0.82[ASN][1000 genomes]
rs28645352	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292014	1.00[ASN][1000 genomes]
rs292034	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292049	1.00[ASN][1000 genomes]
rs292055	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292057	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292060	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292066	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs292068	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs292069	0.80[AMR][1000 genomes]
rs292070	0.81[AMR][1000 genomes]
rs292071	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs292072	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292076	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292078	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292079	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292082	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292084	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs292085	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2943155	0.90[ASN][1000 genomes]
rs2943156	0.90[ASN][1000 genomes]
rs2943157	0.90[ASN][1000 genomes]
rs2943158	0.90[ASN][1000 genomes]
rs2943160	0.82[ASN][1000 genomes]
rs2960592	0.90[ASN][1000 genomes]
rs2995111	0.90[ASN][1000 genomes]
rs4234996	0.82[ASN][1000 genomes]
rs4234997	0.82[ASN][1000 genomes]
rs4280716	0.82[ASN][1000 genomes]
rs4367162	0.82[ASN][1000 genomes]
rs4377578	0.82[ASN][1000 genomes]
rs4605640	0.82[ASN][1000 genomes]
rs4692334	0.82[ASN][1000 genomes]
rs4692335	0.82[ASN][1000 genomes]
rs542264	1.00[ASN][1000 genomes]
rs55684803	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs557255	0.90[ASN][1000 genomes]
rs567993	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569100	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569708	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs611376	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs666451	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs673272	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs687535	1.00[ASN][1000 genomes]
rs7655105	0.82[ASN][1000 genomes]
rs7672198	0.82[ASN][1000 genomes]
rs7695696	0.82[ASN][1000 genomes]
rs7698467	0.82[ASN][1000 genomes]
rs9784504	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:28476600-28484400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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