Variant report

Variant	rs4432834
Chromosome Location	chr5:68299369-68299370
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10035142	0.92[ASN][1000 genomes]
rs10042265	0.93[ASN][1000 genomes]
rs10755226	0.93[ASN][1000 genomes]
rs10805425	0.92[ASN][1000 genomes]
rs10940191	0.92[ASN][1000 genomes]
rs12656917	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12697069	0.89[ASN][1000 genomes]
rs3922936	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3922937	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4269255	0.86[ASN][1000 genomes]
rs4336313	0.88[ASN][1000 genomes]
rs4373240	0.94[ASN][1000 genomes]
rs4443379	0.82[ASN][1000 genomes]
rs4594812	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4976004	0.94[ASN][1000 genomes]
rs4976007	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4976056	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4976057	0.93[ASN][1000 genomes]
rs4976058	0.93[ASN][1000 genomes]
rs4976067	0.92[ASN][1000 genomes]
rs4976068	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5022687	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5022688	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6449989	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6450000	0.93[ASN][1000 genomes]
rs6874327	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6874774	0.93[ASN][1000 genomes]
rs6877507	0.93[ASN][1000 genomes]
rs6877626	0.93[ASN][1000 genomes]
rs6877919	0.93[ASN][1000 genomes]
rs6882278	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6887916	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6888650	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6894214	0.92[ASN][1000 genomes]
rs7446085	0.93[ASN][1000 genomes]
rs7711962	0.93[ASN][1000 genomes]
rs7712326	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7712349	0.93[ASN][1000 genomes]
rs7718238	0.92[ASN][1000 genomes]
rs7718531	0.91[ASN][1000 genomes]
rs7729300	0.93[ASN][1000 genomes]
rs7732664	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7732834	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7733298	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7733454	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7734105	0.91[ASN][1000 genomes]
rs9885496	0.89[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	esv2763462	chr5:68295338-68307023	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	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	chr5:68298000-68301600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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