Variant report

Variant	rs7715730
Chromosome Location	chr5:92502276-92502277
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10428523	0.96[ASN][1000 genomes]
rs11738974	0.96[ASN][1000 genomes]
rs11742251	0.94[ASN][1000 genomes]
rs11743310	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12054781	0.92[ASN][1000 genomes]
rs34700540	0.93[ASN][1000 genomes]
rs4242240	0.97[ASN][1000 genomes]
rs4242241	0.97[ASN][1000 genomes]
rs4242242	0.96[ASN][1000 genomes]
rs4242244	0.81[ASN][1000 genomes]
rs4264926	0.97[ASN][1000 genomes]
rs4266388	0.98[ASN][1000 genomes]
rs4285204	0.97[ASN][1000 genomes]
rs4293897	0.99[ASN][1000 genomes]
rs4302568	0.97[ASN][1000 genomes]
rs4321736	0.96[ASN][1000 genomes]
rs4370258	0.85[ASN][1000 genomes]
rs4449514	0.97[ASN][1000 genomes]
rs4469186	0.97[ASN][1000 genomes]
rs4551050	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4551051	0.97[ASN][1000 genomes]
rs4554194	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4557386	0.96[ASN][1000 genomes]
rs4632783	0.97[ASN][1000 genomes]
rs4869191	0.97[ASN][1000 genomes]
rs4869415	0.97[ASN][1000 genomes]
rs4869417	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55993462	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57542119	0.96[ASN][1000 genomes]
rs59262698	0.96[ASN][1000 genomes]
rs6557066	0.99[ASN][1000 genomes]
rs66467168	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs66624622	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67069214	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67217436	0.97[ASN][1000 genomes]
rs67735054	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67862943	0.96[ASN][1000 genomes]
rs6863269	0.94[ASN][1000 genomes]
rs6897863	0.95[ASN][1000 genomes]
rs7700810	0.96[ASN][1000 genomes]
rs7714485	0.96[ASN][1000 genomes]
rs7722144	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7722718	0.96[ASN][1000 genomes]
rs9764490	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9790989	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9791001	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[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	nsv1029175	chr5:92436038-92548473	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92500800-92521600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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